Clinical Research Manager - Medical Devices - South East UK - to £50K

This innovative, university spin-out medical device company is looking to appoint a new Clinical Research Manager to manage six sites across Europe and Chile.

When you work for this company you become part of an small, highly dedicated, talented team of professionals, committed to quality and passionate about clinical research .

This is a site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close; covers five sites in Europe and one in Chile. Clinical studies will be focused on their cutting edge vascular medical devices.

You must have a significant experience working in the clinical research sector, with experience managing sites from initiation to closeout. Medical device experience is essential and a good understanding of catheterisation laboratory etiquette would be beneficial. You must have excellent attention to detail, experience of CRF completion and have good time management skills.

You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience you will gain an attractive employment package with a competitive salary and the opportunity to join this fast moving company, highly farsighted company.

To discuss this role in more detail please contact Kristina on Kristina@seltekconsultants.co.uk

Job Ref: 8417

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CRA or Senior CRA - Italy - Medical Devices - 8351

The medical devices arm of this global CRO is looking to recruit a senior CRA in Italy.
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Italy. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!

You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Italy. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!

To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk


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CRA or Senior CRA - Spain - Medical Devices - 8350

The medical devices arm of this global CRO is looking to recruit a senior CRA in Spain .
When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Spain. Clinical studies will be focused on their medical devices.
Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!

You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Spain. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!

To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk


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CRA or Senior CRA - France - Medical Devices - 8349

The medical devices arm of this global CRO is looking to recruit a senior CRA in France.

When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in France. Clinical studies will be focused on their medical devices.

Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!

You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in France. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!

To discuss this role in more detail, please contact Kristina on kristina@seltekconsultants.co.uk

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CRA or CRA II - Hungary - 8347

An exciting opportunity has arisen in this leading CRO for a CRA role with clinical responsibility for Hungary!

You will be responsible for leading a team of experienced CRAs across a range of high profile oncology projects! When you work for this medium sized, well respected company you work for a company specialising in supporting the development of new drugs in a wide range of therapeutic areas: oncology in particular, as well as CNS and cardiovascular sciences.

With an international presence and high profile pharmaceutical and biotechnology clients, the company offers an excellent environment in which to develop your career further. In this role you will be responsible for clinical study sites based in Hungary from initial start up through to close out across phase II and III projects with an international scope. Within these projects you will be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships. This company offers excellent training and development to its CRAs, both internally and externally, along with ongoing performance monitoring to help you develop your career, either into clinical management or project management, with the company.

Who are we looking for? You will be an experienced CRA able to demonstrate the ability to manage all aspects of site activity from set up through to close-out in Hungary. Experience in the monitoring of oncology studies is essential. On offer is a competitive renumeration package, excellent training and development, and the opportunity to become part of a talented international team!

For more information or to register your interest please contact Kristina on kristina@seltekconsultants.co.uk
Please note that by applying to this role, you are only expressing your interest; I will discuss the role and company in detail with you before your CV is submitted to our client.


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Manager, Clinical Support - Optometry - Europe - to €70K

This is a rare opportunity to join an innovative ophthalmic medical device company which is developing ground-breaking vision correction technologies for post-cataract surgery patients.

They are looking for an experienced optometry specialist to work with the ophthalmic surgeons throughout Europe and provide technical and application support on this innovative lens which is the only one of its kind on the market.

This position has arisen due to expansion throughout Europe, and you will be involved in working alongside the European team to ensure the surgeons are fully aware of the product's applications.

This lens has been twelve years in development. The company is now moving away from R&D and becoming more commercially active. Europe has a designated Sales Director who is involved in promoting this product throughout Europe, and a Director of Clinical Support who you will report to. You will act as a specialist in Europe for this lens, and be at hand to answer any technical queries regarding the application of this lens.

This company offers a small, friendly working environment. You can be home based anywhere in mainland Europe (in particular Germany, Spain, Italy, France or Czech Republic), and be expected to travel to visit the surgeons on a frequent basis.

The prospects are unlimited in this company, and the role will be what you make it! The company offers a strong support structure, but also the freedom for you to work independently.

So, if you are currently working in optometry, and would like the opportunity to work as a clinical support specialist, then please contact Kristina on Kristina@SeltekConsultants.co.uk for more detail.

Job Ref: 8294

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Medical Representative - Diagnostic Instrumentation - UK - to £38K (£45K OTE)

This global company is looking to hire two medical representatives to join their diagnostic team in the UK.

Territory 1: Southern England (to be based north of the M4)

Territory 2: North West England (Liverpool/Wirral area)

This is a new position created specifically to promote diagnostic instrumentation to primary and secondary care. You will work exclusively for a leading diagnostic company, who are market leaders with a well-known, global brand.

You will promote these instruments to obstetrics and gynaecology consultants in hospitals, as well as key opinion leaders and GP specialists.

You will need to be a dynamic individual who is open minded and flexible. They are looking for someone with secondary care experience (a small amount will be enough) who doesn t mind promoting to specialists in primary care.

In return, you will be given an excellent salary and bonus scheme, as well as a premium car, significantly outside the norm for this level of role! You will also benefit from an excellent pension scheme, healthcare, gym membership and much more!

Job Ref: 8233

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Account Associate - CRO - UK - to £35K

This medium sized global CRO is looking to recruit an Business Development Associate to be based out of their UK office. This is an excellent opportunity to join an expanding company that places the personal development of its employees as a priority.

When you work for this global CRO, you will provide in-house support to the Business Development Director in maintenance of existing accounts, assist in development of new accounts and client management, coordinate sales activities with internal sources including operations and contract management, as well as support in the preparation of materials for capabilities and proposal presentations, marketing search and etc.

This is a great job for someone with a working knowledge of the clinical development process and experience in a previous proposals role (only a small amount of experience is required). Good communication and interpersonal skills are essential to the role as well as exceptional IT skills. You will in return benefit from a competitive salary package and excellent benefits as well as an annual bonus. The company is very eager to get the right person in as soon as possible so call us now to apply!!!

Please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Job Ref: 8228

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Regulatory Executive/Consultant - South East UK - to 45K

This is a varied and challenging Regulatory Executive position with an expert consultancy company based in Cambridgeshire.

You will provide regulatory consultancy services to internal and external clients, including preparation, review, submission and project management of regulatory applications. You will maintain an awareness of, and provide feedback on, client, industry and regulatory developments to input into the strategic development of the department. You will also attend client project meetings, as well as maintaining electronic and hard copy project and regulatory files.

Who are we looking for? You will have experience in a pharmaceutical/healthcare product development environment and have a sound technical and scientific understanding of the clinical development of pharmaceutical/healthcare products. You will need an overall understanding of the drug development process and the role of regulatory affairs within that process

For more information, please contact Kristina on kristina@seltekconsultants.co.uk or 01279 657716

Job Ref: 8217

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Sr Director, Clinical Research, Infectious Disease - to £88K

This top 10 global CRO is looking to recruit a Senior Director of Clinical Research to be based in either UK, Germany or Switzerland. It's an excellent opportunity to join a rapidly expanding company that regards the personal development of its employees as a priority.

You will sit in the clinical research group and act as the interface between the sponsor, the clinical team and the business development team.

You will be responsible for developing existing pharmaceutical relationships and liaise heavily with the BD team and assist in proposals and bid defences.

You will provide direction to the project managers, including supervision, training, and mentoring, and you will also determine headcount needs throughout the department.

You will be involved in developing and/or reviewing SOPs related to the clinical research activities and develop and implement project management principles and tools for use by project managers

The company is looking for an experienced senior project manager, who has extensive knowledge of infectious disease areas. You will need to have experience in business development, or at least be heavily involved in liaising with the BD department. A very generous package is on offer, with the flexibility of working from home if you wish.

Job Ref: 8208

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Director of Clinical Support - Optometry - Europe - to £70K

This is a rare opportunity to join an innovative ophthalmic medical device company which is developing ground-breaking vision correction technologies for post-cataract surgery patients.

They are looking for an experienced optometry specialist to work with the ophthalmic surgeons throughout Europe and provide technical and application support on this innovative lens which is the only one of its kind on the market.

This position has arisen due to expansion throughout Europe, and you will be involved in working alongside the European team to ensure the surgeons are fully aware of the product's applications.

This lens has been twelve years in development. The company is now moving away from R&D and becoming more commercially active. Europe has a designated Sales Director who is involved in promoting this product throughout Europe. You will act as the specialist in Europe for this lens, and be at hand to answer any technical queries regarding the application of this lens.

This company offers a small, friendly working environment. You will report to the CEO, and have input into the development of the company throughout Europe. You can be home based anywhere in Europe (in particular UK, Germany, Spain, Italy, France or Czech Republic), and be expected to travel to visit the surgeons on a frequent basis.

The prospects are unlimited in this company, and the role will be what you make it! The company offers a strong support structure, but also the freedom for you to work independently.

So, if you are currently working in optometry, and would like the opportunity to work as a clinical support specialist, then please contact Kristina on 01279 657716 or email Kristina@SeltekConsultants.co.uk for more detail.

Job Ref: 8198

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Business Development Associate - Proposals - South UK - to £34K

This medium sized global CRO is looking to recruit a Business Development Associate to be part of the proposals team in their UK offices. This is an excellent opportunity to join an expanding company that places the personal development of their employees as a priority.

When you work for this global CRO, you will manage the proposal development process by maintaining deliverables to clients, putting together time and budget estimates and provide analyses for complex, global studies through discussions with senior management, operational teams and sales teams across Europe and globally.

As a Senior BDA you will also train and develop business development associates in procedures, and interdepartmental responsibilities, implement pricing software and coordinate international proposal development and liaison with International Proposal Development.

This is a great job for someone with a working knowledge of the clinical development process and experience in clinical trial time and cost proposal development to move into a more senior position. Good communication and interpersonal skills are essential to the role as well as exceptional IT skills. You will in return profit from a competitive salary package and excellent benefits as well as an annual bonus. The company is very eager to get the right person in as soon as possible so call us now to apply!!!

Please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Job Ref: 8193

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Senior Director of Clinical Research - Western Europe - to £88K

This top 10 global CRO is looking to recruit an Senior Director of Clinical Research to be based in either UK, Germany or Switzerland. This is an excellent opportunity to join a rapidly expanding company that places the personal development of its employees as a priority.

You will sit in the clinical research group and act as the interface between the sponsor, the clinical team and the business development team.

You will be responsible for developing existing pharmaceutical relationships and liase heavily with the BD team and assist in proposals and bid defenses.

You will provide direction to the project managers, including supervision, training, and mentoring and on an ongoing basis, determine headcount needs throughout the department

You will be involved in developing and/or review SOPs related to the clinical research activities and develop and implement project management principles and tools for use by Project Managers

They are looking for an experienced senior project manager, who has extensive knowledge of either oncology or neuroscience. You will need to have experience in BD, or at least heavily involved in liasing with the BD department. A very generous package is on offer, with the flexibility of working from home if you wish.

Job Ref: 8179

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Senior Quality Assurance Auditor - Eastern Europe - CRO

One of the leading and fastest growing global clinical research organisations (CROs) is looking to recruit Senior Quality Assurance Auditors in either Hungary, Czech Republic, Romania, Serbia, Bulgaria or Ukraine . This is an exciting opportunity for you to work for a multinational company that offers the great progression opportunities

As an experienced GCP auditor from any of the countries above, you will be required to conduct three audits per month which include audits of investigator sites and vendors, document/TMF audits, trusted process audits, hosting sponsor audits and co-visit audits with clinical research associates (CRAs).

You will responsible for mentoring less experienced QA auditors, and have the opportunity to act as a lead auditor on team audits and project audits.

You must be able to demonstrate strong and comprehensive knowledge of Good Clinical Practice (GCP) regulations and guidelines and have good experience as an auditor as well as a strong grasp of medical terminology.

A competitive remuneration package is on offer, as well as the opportunity to work for this leading, global CRO.

For more information, please email Kristina, at kristina@seltekconsultants.co.uk

Please note that applying to this job only expresses interest; we will not send your CV to the company without first discussing the role and position in detail with you

Job Ref: 8168

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Medical Monitor - Slovakia - to €57K

This global clinical research organisation (CRO) is looking to recruit a Medical Monitor in Slovakia. This company prides itself in being highly scientifically developed, with strong scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has a very evolved training system in place which means great career development opportunities for you!.

You will benefit from a supportive career development environment, a competitive remuneration package and a fun and supportive team atmosphere.

You will be responsible for Medically managing clinical trials as well as collaborating with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)

You will also provide therapeutic and protocol-specific training to the project teams as well as contributing to the medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc

You will support Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management

You will also have the opportunity to assist in the mentoring of medical staff (nurses, junior physicians, etc)

You must be educated to Medical Degree level from an accredited institution of Medical Education, with some experience in the clinical research industry

For more information or to apply to this role, please email Kristina on kristina@seltekcosultants.co.uk or call 0044 1279 657716

Job Ref: 8147

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Medical Monitor - Czech Republic - to €70K

This global clinical research organisation (CRO) is looking to recruit a Medical Monitor in the Czech Republic. This company prides itself in being highly scientifically developed, with strong scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has a very evolved training system in place which means great career development opportunities for you!.

You will benefit from a supportive career development environment, a competitive remuneration package and a fun and supportive team atmosphere.

You will be responsible for Medically managing clinical trials as well as collaborating with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)

You will also provide therapeutic and protocol-specific training to the project teams as well as contributing to the medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc

You will support Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management

You will also have the opportunity to assist in the mentoring of medical staff (nurses, junior physicians, etc)

You must be educated to Medical Degree level from an accredited institution of Medical Education, with some experience in the clinical research industry

For more information or to apply to this role, please email Kristina on kristina@seltekcosultants.co.uk or call 0044 1279 657716

Job Ref: 8146

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Senior CRA or CRA II - South East UK - to £34K

An exciting opportunity has arisen in this leading CRO for a Senior CRA role with UK wide clinical responsibility!

You will be responsible for leading a team of experienced CRAs across a range of high profile oncology projects! When you work for this medium sized, well respected company you work for a company specialising in supporting the development of new drugs in a wide range of therapeutic areas: oncology in particular, as well as CNS and cardiovascular sciences.

With an international presence and high profile pharmaceutical and biotechnology clients, the company offers an excellent environment in which to develop your career further. In this role you will be responsible for clinical study sites based in the UK from initial start up through to close out across phase II and III projects with an international scope. Within these projects you will be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships. As a Senior CRA you will also act as local country co-ordinator for all site level activities in the UK, supporting other local CRAs. This company offers excellent training and development to its CRAs, both internally and externally, along with ongoing performance monitoring to help you develop your career, either into clinical management or project management, with the company.

Who are we looking for? You will be an experienced CRA able to demonstrate the ability to manage all aspects of site activity from set up through to close-out in the UK. Experience in the monitoring of oncology studies is essential. On offer is a competitive renumeration package, excellent training and development, and the opportunity to become part of a talented international team!

For more information or to register your interest please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Please note that by applying to this role, you are only expressing your interest; I will discuss the role and company in detail with you before your CV is submitted to our client.

Job Ref: 8142

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Feasibility Analyst - CRO - South East UK - to £27K

This global, medium sized, full service CRO are looking to hire a Feasibility Analyst to join their offices in the UK

You will be responsible for collection, analysis and presentation of feasibility data for both country and site level. This will be for projects won or yet to be won.

You will be responsible for ensuring swift progress through the feasibility process, which will include duties such as collaboration with Business Development, Business Analysts and other departments, designing protocol specific site level feasibility questionnaires, analysing the data to provide the report to the trial managers, as well as writing up feasibility results and recommendations on the strategic patient recruitment plan.

The ideal candidate will have experience in the clinical research industry, looking to move into an exciting position in a company who put their employees personal develop one of their top priorities.

For more information, please email Kristina@SeltekConsultants.co.uk or call 01279 657716

Job Ref: 8141

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Quality Compliance Associate - UK to £27K (£28K OTE)

One of the largest and most recognised manufacturers of life science research products has created a new opportunity within its European compliance team. The role will be office based in the South West of the UK.

This is a dynamic and challenging role, which involves understanding the evolving compliance offer, its role as a sales tool and delivering a compliance support service to customers by adopting a consultative approach. You will be part of a small UK team supporting all compliance issues, you will need to liase with a variety of other departments and take responsability for handling to conclusion queries.

The successful candidate will be a life science graduate with great attention to detail and a tenacious character. Previous experience of using SAP based systems would be helpful however full training and support can be provided to ensure you are confident in the role. To discuss this great opportunity in detail contact us soon.

Job Ref: 8138

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Senior Drug Safety Associate - South UK - to £35K

This is an exciting opportunity for a Drug Safety Associate to join one of the leading international clinical research organisations (CROs).

You will be involved in reviewing SAE information from investigator sites and AEs from post marketing sources for completeness and regulatory compliance, as well as perform QC reviews of safety reports and preparing safety data reports for submissions to clients.

Because of the level of seniority of the position, you will be in contact with clinical operations personnel and clients to ensure compliance with safety and pharmacovigilance SOP as well as mentoring safety associates and other members of the safety and pharmacovigilance team.

Excellent training is provided and there is plenty of scope for development into more senior positions.

Who are we looking for? You will have a proven track record of working in drug safety and pharmacovigilance. A strong scientific or nursing background is essential for success in this role (equivalent experience will be considered).

For more information, please email Kristina at kristina@seltekconsultants.co.uk

Please note, that applying for this opportunity only expresses interest; we will discuss the role and company in detail with you before your CV is sent to the company.

Job Ref: 8083

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Clinical Research Associate - UK - to £35K

This is a varied and challenging Clinical Research Associate (CRA) or Senior Clinical Research Associate (SCRA) position with an expert consultancy company!

Broaden your scientific knowledge within clinical research by working on novel studies in phase I-II and Proof of Concept stages of development! When you work for this small but expanding speciality company you take on a broad set of responsibilities ranging from protocol and Investigator Brochure development through to business operations and training!

You ll gain broader exposure in this company than with any other business in the clinical research industry! Based from the office in East Anglia you will work as part of small, highly experienced and dedicated team to deliver clinical projects on time and within budget.

In this small company the CRA and SCRA roles involve site management and monitoring in the UK; study design and set up; the development of regulatory documentation such as investigator brochures, protocols, informed consent and clinical study reports; and business operations activities to include client relationship management, business development and marketing. At the CRA level you will focus mainly on the site management and co-ordination activities and at SCRA level you will be more involved in local project management activities and the development of regulatory documentation in addition to managing sites.

Who are we looking for? With a strong scientific background you will have a proven track record in the management and monitoring of UK sites. Exposure to phase I/II and Proof of Concept is an advantage. Your experience could come from academia, CRO or pharmaceutical/biotechnology company environments.

For more information, please email Kristina on kristina@seltekconsultants.co.uk or call 01279 657716

Job Ref: 8132

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Clinical Project Manager - South East UK - to £55K

This rapidly growing global CRO is urgently looking for a Project Manager to work from their offices in the UK. You will be responsible for overseeing and coordinating the operational aspects of assigned project personnel on ongoing projects. As the primary liaison between the CRO and your clients, you will need to ensure that you have a good understanding of the clients' expectations and that their goals of time, cost, and quality performance are met. This role gives you the opportunity to really get stuck in!! Working on multiple projects at any given time you will be responsible for the cross functional management of the project team! Other responsibilities include budgetary control; coordination and drafting of contracts with external providers and investigators; overseeing the regulatory document collection and submission process; coordination of the data cleanup between clinical operations, data management, biostatistics, and medical affairs; training and mentoring of project managers, and much, much more!

You will be educated to degree level and currently be working within the industry. Project management experience is essential!! Knowledge and experience with FDA/ICH/ISO14155 regulations, drug development and clinical monitoring procedures are necessary. You will be confident and possess strong interpersonal, decision making and strong leadership skills. You will need to be flexible to travel. For your efforts you will be rewarded with an excellent salary and benefits package!

Call Kristina on 01279 657716 and kristina@seltekconsultants.co.uk

Job Ref: 8125

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Senior CRA / CRA II - France - to €40K

This global CRO is looking to recruit a senior CRA in France.

When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in France. Clinical studies will be focused on their Oncology and CNS studies.

Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!

You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in France. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!

For more information, please call kristina on 0044 1279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8124

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Senior CRA - Benelux - to €65K

This global CRO is looking to recruit a senior CRA in Belgium or the Netherlands.

When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is site co-ordination role in which you will manage all site related activities from protocol review and feasibility through to close out locally in Benelux. Clinical studies will be focused on their Oncology and CNS studies.

Additional responsibilities will include mentoring/coaching junior CRAs, local project management activities and some international liaising at site level - there will also be the chance to take on lead duties within specific projects. This is an excellent opportunity to work for a medium sized CRO that places their employees career progression as their number one priority!

You will have a scientific background and proven track record of start up, initiation, monitoring and close out activities in Benelux. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team!

For more information, please call Kristina on 0044 1279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8123

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Study Start-Up Manager - Germany - to €63K

This is a rare opportunity at a small/medium sized global CRO to be a Study Start-up Manager based in Germany

As Start-up Manager you will be the cornerstone of a smooth-running clinical operation and amongst many other responsibilities you will make sure that ethics applications for all on-going projects are approved. You will also be involved in feasibility strategy, helping junior CRAs with finding new sites, line-managing CTAs, dealing with principal investigators and liaising with sponsors for feedback. This rapidly growing CRO is keen to find the right person to keep things on track and make sure that new projects start up without a hitch.

To be successful you will need a strong background in clinical research, with experience in feasibility, site selection and initialtion.This is the perfect opportunity for a CRA who wants career progression but does not necessarily want to be a PM. There is also some flexibility to work from home.

To learn more, or to discuss your application in confidence, please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8119

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Senior QA Auditor - Medical Devices - Germany or Switzerland

This expanding, global CRO is looking to recruit a Senior QA Auditor - Medical Devices to be based in either Germany or Switzerland In this role you will conduct all aspects of internal and external auditing, to include sponsor and investigator audits, to ICH GCP and ISO14155 for the company's medical device studies.

Audits will be system, process, facility, documentation and site focused, across Europe. In addition to your auditing duties you will have the chance to get involved in supervising a junior QA Auditor, with a view to taking on line management responsibilities and a QA Manager role in the near future.

Who are we looking for? A scientific background is essential along with a proven track record of medical device auditing to ICH GCP requirements. Full training will be provided to candidates with strong ICH GCP auditing experience. Practical experience with all types of internal and external audit is essential. A competitive salary and remuneration package is available to the successful candidate. If you are looking to broaden your auditing experience within clinical trials then please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Please note that your details will kept entirely confidential, and we will contact you prior to sending your CV to any company.

Job Ref: 8118

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Senior QA Auditor - Spain, Italy or France - to €50K

This expanding, global CRO is looking to recruit a Senior QA Auditor to be based in either Spain, Italy or France. In this role you will conduct all aspects of internal and external auditing, to include sponsor and investigator audits, to ICH GCP and ISO14155.

Audits will be system, process, facility, documentation and site focused, across Europe. In addition to your auditing duties you will have the chance to get involved in supervising a junior QA Auditor, with a view to taking on line management responsibilities and a QA Manager role in the near future.

This is an excellent opportunity to gain QA expertise within another area of clinical product development, whilst at the same time gaining valuable leadership and management skills for the future!

Who are we looking for? A scientific background is essential along with a proven track record of auditing to ICH GCP requirements. Full training will be provided to candidates with strong ICH GCP auditing experience. Practical experience with all types of internal and external audit is essential. A competitive salary and remuneration package is available to the successful candidate. If you are looking to broaden your auditing experience within clinical trials then please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Please note that your details will kept entirely confidential, and we will contact you prior to sending your CV to any company.

Job Ref: 8117

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Clinical Study Leader - Pharma - UK to £45K

Clinical Study Leader / Clinical Project Manager

There is an opportunity for a Study Leader to join this dynamic, cutting edge pharmaceutical company. You will be responsible for the execution of Phase 3 and other approved clinical studies, which will include the overall management of clinical studies from study design to clinical report finalisation, ensuring that the studies are conducted to the highest quality standards, are within the agreed budget and are delivered on time.

You will be involved in planning clinical studies with the rest of the team, writing documents (protocols, etc), overseeing monitoring and evaluating and selecting study investigators. You will be involved in investigator meetings as well as managing timelines of protocol development, study conduct, database lock, statistical outputs and delivery of study reports.

You will need to be educated to BSc level and have broad experience monitoring gained over a few years. You must have some experience in managing clinical trials (either in a JrPM role or CRA role). Phase 3 clinical study management would be beneficial.

For more information, please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Job Ref: 8114

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Senior CRA - UK - Home Based - to £45K

This global clinical research organisation (CRO) is looking to recruit a Senior CRA in the UK. This company prides itself in being highly scientifically developed, with strong scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has a very evolved training system in place which means great career development opportunities for you!.

You will benefit from a supportive career development environment, a competitive remuneration package and a fun and supportive team atmosphere.

You will be responsible for site feasibility, initiation, management and close-out visits for the studies. You will function as Lead CRA for global studies, coordinating CRAs, reviewing monitoring reports etc. when required. You will have the opportunity to mentor and train colleagues and site staff when needed as well as designing monitoring plans and supporting in the design of the protocols and CRFs

Experience of monitoring cardiovascular studies will be essential. In return, you will benefit from a competitive remuneration package and strong career growth potential.

Please apply or for more information email kristina@seltekconsultants.co.uk or call Kristina on 01279 657716

Job Ref: 8113

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Clinical Project Manager - CNS - Europe - to €70K

This leading, global clinical research organisation (CRO) is looking to recruit a Project Manager to manage various CNS clinical research projects throughout Europe. This position has arisen due to expansion, as they have recently won a large number of CNS proposals and are looking for someone to take control of the projects. You can be based in any European country for this role.

This is an expanding, dynamic CRO that has tripled in size in Europe over the last three years. Specialising in the development of oncology, CNS, anti-infective and cardiovascular products they offer a comprehensive range of services to small and medium sized biotech and pharmaceutical companies. This company focuses on its people, offering excellent training and development opportunities and a fun, team focused working environment.

You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRFs and SAE reports.

You will also plan, coordinate, and present at investigators meetings, participate in proposal meetings with potential clients as well as prepare project management reports for clients, project personnel, and the company s management team.

You must be educated to BSc level or RGN, and have a successful background in managing international projects. You can be based in almost any European country.

To discuss this role in confidence, please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8108

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Senior Compliance Associate - QA (GLP and GCLP) - UK - to £41K

One of the leading global CROs is looking to recruit a Senior Compliance Associate to join the QA department in the UK.

You will be responsible for GCLP and GLP audits, QA reviews and evaluations and writing of SOPs. You will also provide training of GCLP and GLP regulations.

You will be required to provide input and assistance to Business Development for time and cost proposal development and provide project management oversight for compliance-related tasks and programs.

To be successful in this role you must have experience in a similar position in clinical research, regulatory affairs or a relevant healthcare research position. You must have relevant GLP and GCLP audit work experience ideally gained in a CRO

You will be required to travel up to 40% of the time, and have the motivation and drive to work independently.

A competitive remuneration package is available, as well as the opportunity to work for this exciting, well respected CRO.

For more information, please email Kristina on kristina@seltekconsultants.co.uk

Please note that applying to this role only expresses interest. We will discuss the role and company with you in detail before we send your CV.

Job Ref: 8090

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Senior Quality Assurance Auditor - Clinical Research - Eastern Europe

One of the leading and fastest growing global clinical research organisations (CROs) is looking to recruit Senior Quality Assurance Auditors in Hungary, Czech Republic, Romania, Serbia, Bulgaria or Ukraine . This is an exciting opportunity for you to work for a multinational company that offers the great progression opportunities

As an experienced GCP auditor from any of the countries above, you will be required to conduct three audits per month which include audits of investigator sites and vendors, document/TMF audits, trusted process audits, hosting sponsor audits and co-visit audits with clinical research associates (CRAs).

You will responsible for mentoring less experienced QA auditors, and have the opportunity to act as a lead auditor on team audits and project audits.

You must be able to demonstrate strong and comprehensive knowledge of Good Clinical Practice (GCP) regulations and guidelines and have good experience as an auditor as well as a strong grasp of medical terminology.

A competitive remuneration package is on offer, as well as the opportunity to work for the leading, global CRO.

For more information, please email Kristina, at kristina@seltekconsultants.co.uk

Please note that applying to this job only expresses interest; we will not send your CV to the company without first discussing the role and position in detail with you.

Job Ref: 8085

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CRA II Serbia - to €30K

This sophisticated and innovative global clinical research organisation (CRO) is looking to recruit a Clinical Research Associate (CRA II) in Serbia . This company prides itself in being scientifically strong with powerful scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has an in-depth training system in place which means excellent career development opportunities for you!

If you are an experienced monitor looking for the next step up in this global, expanding and dynamic company, then please apply or email Kristina@seltekconsultants.co.uk.

Job Ref: 8013

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Freelance CRA - 1FTE or 0.5FTE France

This sophisticated and innovative global clinical research organisation (CRO) is looking to recruit a Freelance Clinical Research Associate France. This company prides itself in being scientifically strong with powerful scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

They are looking for a 1FTE CRA with CNS experience and 0.5FTE with cardiology experience. The contract will be initially 3 months.

If you are an experienced monitor looking for the next step up in this global, expanding and dynamic company, then please apply or email Kristina@seltekconsultants.co.uk.

Job Ref: 8104

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Senior QA Auditor - CRO - South UK - to £50K

This expanding, global CRO ware looking to recruit a SrQA Auditor to join their offices in the UK.

In this role you will conduct all aspects of internal and external auditing, to include sponsor and investigator audits, to ICH GCP and ISO14155. Audits will be system, process, facility, documentation and site focused, across Europe. In addition to your auditing duties you will have the chance to get involved in supervising a junior QA Auditor, with a view to taking on line management responsibilities and a QA Manager role in the near future. This is an excellent opportunity to gain QA expertise within another area of clinical product development, whilst at the same time gaining valuable leadership and management skills for the future! Who are we looking for? A scientific background is essential along with a proven track record of auditing to ICH GCP requirements. The ideal candidate would have some exposure to device trials and auditing to ISO 14155 requirements. Full training will be provided to candidates with strong ICH GCP auditing experience looking for a move into devices. Practical experience with all types of internal and external audit is essential. A competitive salary and remuneration package is available to the successful candidate. If you are looking to broaden your auditing experience within clinical trials then please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Job Ref: 8103

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CTA-II / Senior CTA - Poland - Polish Zloty 78,000

An experienced career CTA is required for an expanding, people focused company! In this role, which is based in Warsaw, Poland , you will support project teams by assisting in the internal organisation of phase II-IV European projects across a range of therapy areas that includes oncology. You will be the central point of contact for all team members regarding the study master file and essential documents and will also track and monitor the status of document retrieval, patient recruitment, payments and monitoring visits. This is an administrative position with some travel to site to co-monitor with CRAs.

Who should apply? If you have previous experience of at least six months in clinical research as a CTA we want to hear from you! You must have excellent IT skills and be quality/detail oriented. Good prospects are available for the future and you will be paid well!

Please call Kristina on 0044 1279 657716 or email kristina@seltekconsultants.co.uk for more details

Job Ref: 8101

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CRA - Czech Republic - to Czech Crown 660,000

A Clinical Research Associate (CRA) position has become available in the Czech Republic with an up and coming, people focused drug development company! When you work for this company you become part of an expanding, talented team of professionals, committed to quality and passionate about clinical research! This is a core monitoring role with additional site management responsibility for hospital and clinic based sites across Czech Republic. Clinical studies will be phase II-IV focused and in the oncology, cardiovascular and CNS therapy areas. Additional responsibilities will include start up activities such as feasibility, local ethics/regulatory applications and the preparation of essential documents. Excellent training and development opportunities will be available to you including promotion to Senior Clinical Research Associate SCRA, involvement in mentoring/training junior Clinical Research Associate CRAs and gaining experience of site co-ordination on an international level.

Who are we looking for? You will have a scientific background and a proven track record of monitoring at site in the Czech Republic. You will be able to work as part of a small team as well as independently with minimal supervision. Flexibility to travel is essential in this role. In return for your experience is a competitive remuneration package and the opportunity to work with a highly experienced and fun team! Call Kristina on 0044 1279 657716 or email kristina@seltekconsultants.co.uk

Job Ref: 8100

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Business Development Associate - Proposals - South UK - to £34K

This medium sized global CRO is looking to recruit a Business Development Associate to be part of the proposals team in their UK offices. This is an excellent opportunity to join an expanding company that places the personal development of their employees as a priority.

When you work for this global CRO, you will manage the proposal development process by maintaining deliverables to clients, putting together time and budget estimates and provide analyses for complex, global studies through discussions with senior management, operational teams and sales teams across Europe and globally.

As a Senior BDA you will also train and develop business development associates in procedures, and interdepartmental responsibilities, implement pricing software and coordinate international proposal development and liaison with International Proposal Development.

This is a great job for someone with a working knowledge of the clinical development process and experience in clinical trial time and cost proposal development to move into a more senior position. Good communication and interpersonal skills are essential to the role as well as exceptional IT skills. You will in return profit from a competitive salary package and excellent benefits as well as an annual bonus. The company is very eager to get the right person in as soon as possible so call us now to apply!!!

Please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Please note that applying to this job only expresses interest; we will not send your CV to the company without first discussing the role and position in detail with you.

Job Ref: 8092

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Business Development Associate II - BD Department - South UK - to £34K

This medium sized global CRO is looking to recruit an Business Development Associate to be based out of their UK office. This is an excellent opportunity to join an expanding company that places the personal development of its employees as a priority.

When you work for this global CRO, you will provide in-house support to the Business Development Director in maintenance of existing accounts, assist in development of new accounts and client management, coordinate sales activities with internal sources including operations and contract management, as well as support in the preparation of materials for capabilities and proposal presentations, marketing search and etc.

This is a great job for someone with a working knowledge of the clinical development process and experience in a previous business development role (only a small amount of experience is required). Good communication and interpersonal skills are essential to the role as well as exceptional IT skills. You will in return benefit from a competitive salary package and excellent benefits as well as an annual bonus. The company is very eager to get the right person in as soon as possible so call us now to apply!!!

Please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk

Please note that applying to this job only expresses interest; we will not send your CV to the company without first discussing the role and position in detail with you.

Job Ref: 8091

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Senior Compliance Associate - QA (GLP and GCP) - South UK - to £39K

One of the leading global CROs is looking to recruit a Senior Compliance Associate to join the QA department in the UK.

You will be responsible for GCP and GLP audits, QA reviews and evaluations and writing of SOPs. You will also provide training of GCP and GLP regulations.

You will be required to provide input and assistance to Business Development for time and cost proposal development and provide project management oversight for compliance-related tasks and programs.

To be successful in this role you must have experience in a similar position in clinical research, regulatory affairs or a relevant healthcare research position. You must have relevant GLP and GCP audit work experience ideally gained in a CRO

You will be required to travel up to 40% of the time, and have the motivation and drive to work independently.

A competitive remuneration package is available, as well as the opportunity to work for this exciting, well respected CRO.

For more information, please email Kristina on kristina@seltekconsultants.co.uk

Please note that applying to this role only expresses interest. We will discuss the role and company with you in detail before we send your CV.

Job Ref: 8090

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Senior Clinical Research Associate (SrCRA) - South UK to £40K

There is an exciting opportunity to join a leading Global CRO as a Senior CRA. This CRO is continuing to grow and develop internationally, and offers good opportunity to progress within the company.

This full-service international CRO specialises in various therapeutic areas including Cardiology, Inflammatory and Oncology, and offers a very competitive remuneration package. This position will be working on new phase I studies in renal and cardiovascular indications. Experience monitoring these types of trials would be an advantage.

They are looking for someone to hit the ground running, so you must be an experienced monitor. Ideally someone currently working as a SrCRA, however, if you have Senior CRA duties in your current position, you will also be considered.

A medical background will be required, either academically or as a RGN.

Job Ref: 8086

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Senior Quality Assurance Auditor - Eastern Europe

One of the leading and fastest growing global clinical research organisations (CROs) is looking to recruit Senior Quality Assurance Auditors in Hungary, Czech Republic, Romania, Serbia, Bulgaria or Ukraine . This is an exciting opportunity for you to work for a multinational company that offers the great progression opportunities

As an experienced GCP auditor from any of the countries above, you will be required to conduct three audits per month which include audits of investigator sites and vendors, document/TMF audits, trusted process audits, hosting sponsor audits and co-visit audits with clinical research associates (CRAs).

You will responsible for mentoring less experienced QA auditors, and have the opportunity to act as a lead auditor on team audits and project audits.

You must be able to demonstrate strong and comprehensive knowledge of Good Clinical Practice (GCP) regulations and guidelines and have good experience as an auditor as well as a strong grasp of medical terminology.

A competitive remuneration package is on offer, as well as the opportunity to work for the leading, global CRO.

For more information, please email Kristina, at kristina@seltekconsultants.co.uk

Job Ref: 8085

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Senior Drug Safety Associate - South UK - to £35K

This is an exciting opportunity for a Drug Safety Associate to join one of the leading international clinical research organisations (CROs).

You will be involved in reviewing SAE information from investigator sites and AEs from post marketing sources for completeness and regulatory compliance, as well as perform QC reviews of safety reports and preparing safety data reports for submissions to clients.

Because of the level of seniority of the position, you will be in contact with clinical operations personnel and clients to ensure compliance with safety and pharmacovigilance SOP as well as mentoring safety associates and other members of the safety and pharmacovigilance team

Excellent training is provided and there is plenty of scope for development into more senior positions.

Who are we looking for? You will have a proven track record of working in drug safety and pharmacovigilance. A strong scientific or nursing background is essential for success in this role (equivalent experience will be considered).

For more information, please email Kristina at kristina@seltekconsultants.co.uk

Please note, that applying for this opportunity only expresses interest; we will discuss the role and company in detail with you before your CV is sent to the company.

Job Ref: 8083

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International Clinical Project Manager - Europe - to €65K

This sophisticated and innovative global CRO is looking to recruit a Clinical Project Manager to take control of their anti-inflammatory projects throughout Europe. This company prides itself in being scientifically strong with powerful scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has an in-depth training system in place which means excellent career development opportunities for you! They work on a competency based promotion structure, which means your progression will be based on ability not number of years of service.

You will be responsible for the overall coordination and management of the trials from the technical and financial to the operational aspects of the projects. You will be responsible for planning and implementation of strategy to ensure that all projects meet the clients expectations

If you have managed international anti-inflammatory projects and are looking to work for an expanding and dynamic company, then please apply or email Kristina@seltekconsultants.co.uk

Please note that applying to this job only expresses interest; we will not send your CV to the company without first discussing the role and position in detail with you.

Job Ref: 8077

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Senior CRA - Sweden - Part Time (0.6FTE) - to 330K SEK per year

This sophisticated and innovative global contract research organisation (CRO) is looking to recruit a Clinical Research Associate (CRA) in Sweden . This company prides itself in being scientifically strong with powerful scientific backing. They also have great expertise in the drug development process but focus mainly on CNS, cardiovascular and inflammatory areas.

This CRO has a lower than average staff turnover, and also has an in-depth training system in place which means excellent career development opportunities for you!

This is a part time, permanent role, with FTE of 0.6. You will be involved in the monitoring of the CNS projects throughout Sweden, In this role you will be responsible for clinical study sites from initial start up through to close out and be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships.

If you are an experienced monitor looking for the next step up in this global, expanding and dynamic company, then please apply or email Kristina@seltekconsultants.co.uk

Job Ref: 8070

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Senior Clinical Research Associate (SCRA) - UK - to £36K

An exciting opportunity has arisen in this leading CRO for a Senior CRA role with UK wide clinical responsibility!

You will be responsible for leading a team of experienced CRAs across a range of high profile oncology projects! When you work for this medium sized, well respected company you work for a company specialising in supporting the development of new drugs in a wide range of therapeutic areas: oncology in particular, as well as CNS and cardiovascular sciences.

With an international presence and high profile pharmaceutical and biotechnology clients, the company offers an excellent environment in which to develop your career further. In this role you will be responsible for clinical study sites based in the UK from initial start up through to close out across phase II and III projects with an international scope. Within these projects you will be responsible for all site management and core monitoring activities, site specific training, clinical site budgets and management of site level relationships. As a Senior CRA you will also act as local country co-ordinator for all site level activities in the UK, supporting other local CRAs. This company offers excellent training and development to its CRAs, both internally and externally, along with ongoing performance monitoring to help you develop your career, either into clinical management or project management, with the company.

Who are we looking for? You will be an experienced CRA able to demonstrate the ability to manage all aspects of site activity from set up through to close-out in the UK. Experience in the monitoring of oncology studies is essential. On offer is a competitive renumeration package, excellent training and development, and the opportunity to become part of a talented international team!

For more information or to register your interest please call Kristina on 01279 657716 or email kristina@seltekconsultants.co.uk

Please note that by applying to this role, you are only expressing your interest; I will discuss the role and company in detail with you before your CV is submitted to our client.

Job Ref: 8067

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