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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