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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