Temporary and Contract Clinical Research Jobs


Examples of contract and temporary clinical vacancies we've handled in the past. You can find all our current vacancies by logging in.

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Salary and benefits for contractors

 

Job Title Clinical Development Advisor
Salary An excellent remuneration package is on offer to the right candidate.
Benefits This is an exciting opportunity to join one of the world's leading blue chip pharmaceutical companies on a 12 month contract.
Duration One year. This rôle may be extended into a long term 'rolling contract' subject to satisfactory performance.
Location Surrey
Job

Our client, an organisation with an impressive product portfolio spanning a range of indications, is looking for a Clinical Development Advisor to complement their medical affairs team. In this rôle you will be responsible for the planning, design and execution of local phase II-IV studies in the rheumatology/dermatology/respiratory therapeutic areas. This challenging rôle also offers the opportunity to become involved with product licensing and NICE applications, training/mentoring of CRAs and the provision of site support to projects.

Experience

The ideal candidate will have have a minimum of 3-4 years experience as a CRA co-ordinating phase II-IV clinical trials. Previous experience with rheumatology/dermatology/respiratory trials essential. BSc life science or related, PhD preferred.

 

Job Title Clinical Development Advisor (part time)
Salary An excellent remuneration package is on offer to the right candidate.
Benefits

This is an exciting opportunity to join one of the world's leading blue chip pharmaceutical companies on a part-time 'maternity cover' contract.

 

Duration Ongoing
Location Surrey
Job

Our client, an organisation with an impressive product portfolio spanning a range of indications, is looking for a Clinical Development Advisor to complement their medical affairs team. In this rôle you will be responsible for the planning, design and execution of local phase II-IV studies in the rheumatology/dermatology/respiratory therapeutic areas. This challenging rôle also offers the opportunity to become involved with product licensing and NICE applications, training/mentoring of CRAs and the provision of site support to projects.

Experience

The ideal candidate will have have a minimum of 3-4 years experience as a CRA co-ordinating phase II-IV clinical trials. Previous experience with rheumatology/dermatology/respiratory trials essential. BSc life science or related, PhD preferred.

 

 

 

Job Title
Clinical Trial Assistant
Salary
Negotiable
Benefits Move into clinical research!!!
Duration 6 - 12 months
Location
South East
Job

Our client, a leading biopharmaceutical company with an interest in oncology, is looking for a Contract CTA to join their clinical team. The contract term will initially be for 6 -12 months, but it is anticipated that this will be extended to become a rolling contract. This is an excellent opportunity to either gain experience in clinical research or to build upon existing basic knowledge. In this rôle you will be responsible for the maintenance of study master files, ensuring that all clinical and regulatory documentation is collected in accordance with ICH GCP guidelines. In addition to this, you will also be resonsible for tracking the collection of these documents, ensuring that they are retrieved from study site within designated timelines. The CTA role provides an excellent introduction to the industry, and will allow the successful candidate to gain valuable experience that can be used as a route into a CRA rôle.

Experience

The ideal candidate will have either a BSc in a life science or related area OR a minimum of 6 months experience in a similar rôle. An attractive salary and benefits package is on offer, including holiday pay and private healthcare.

 

Job Title
Clinical Research Associate
Salary
£27,000 basic
Benefits A competitive benefits package is on offer including healthcare, car allowance and holiday pay.
Duration Six months
Location
Scotland
Job

Our client, a leading pharmaceutical company with an interest in cardiovascular, diabetes and oncology research, is looking for a contract CRA to cover maternity leave for a period of 6 months. This contract may be extended to become a long term 'rolling' contract as project demands increase. You would take over an existing cardiovascular project, managing all site activities for assigned centres in Scotland, ensuring ICH GCP compliance. This is an excellent opportunity to experience clinical trial co-ordination within a pharmaceutical environment and will allow the successful candidate to build upon exisitng therapeutic area knowledge.

Experience

The ideal candidate will have a minimum of 12 months experience monitoring in the field. Experience with phase II/III cardiovascular trials is desirable, as a BSc in a life science or RGN qualification.

 

Job Title Clinical Research Assistant
Salary To be agreed
Benefits There is an excellent remuneration and benefits package on offer to the right candidate
Duration One year
Location Field based - UK
Job

Our client, one of the top 10 blue chip pharmaceutical companies, is looking for a field based contract CRA to join their clinical team. The contract term is initially for 12 months, although this wil be renewed on a 'rolling contract' basis and is essentially open-ended. This is an excellent opportunity to gain experience working within a pharmaceutical environment on a contract basis whilst enjoying many of the benefits, training and potential for promotion offered to permanent employees.

Experience

The ideal candidate will have a minimum of 12 months monitoring experience, and will be familiar with the activities relating to site initiation, management and closure.

 

Job Title Senior CRA
Salary To be agreed
Benefits A competitive salary and benefits package is on offer including holiday pay, car allowance and healthcare.
Duration One year
Location Field based - UK
Job

This is an excellent opportunity to gain experience working on a wide range of projects in some of the most exciting therapeutic areas within a pharmaceutical company. Our client, a market leader in drug discovery and development, has a requirement for a Senior CRA to join their operations team, initially on a 12 month contract. The position is to be field based in the UK, and although the contract term is initially 12 months in duration, this will be extended on a 'rolling contract' basis subject to satisfactory performance. In this rôle you will be responsible for the site management and monitoring of a number of projects in phases II-IV of development. There will also be the opportunity to become involved in regional project management.

Experience

The ideal candidate will have a minimum of three years experience as a CRA, and MUST have set up, initiated, and closed down study sites. Also required is broad therapeutic area experience.

 

Job Title Project Leader
Salary To be agreed
Benefits

Move into people management!! An excellent remuneration package is on offer with benefits including healthcare, holiday pay, car allowance.

Duration Long term rolling contract
Location Kent
Job

Our client, one of the worlds leading blue chip pharmaceutical companies, requires a Project Leader to work on a long term 'rolling contract' basis. The rôle is to be office based in the south of the UK, managing clinical trials in a wide range of therapeutic area's to ICH GCP. In this rôle you will be involved in feasibility studies, project timeline planning and other project management activites. You will be assigned several projects in a wide range of therapeutic areas and phases of clinical development, allowing you to expand upon your existing knowledge and gain experience of the most exciting therapeutic areas. This is an excellent opportunity to work in a balanced environment that values clinical professionalism and medical ethics.

Experience

The requirements for this position are a minimum of 3-4 years experience as a CRA and a thorough working knowledge of clinical trial design and development in a wide range of therapeutic areas. Must be familiar with the management of clinical budgets.

 

Job Title CRA/SCRA North West
Salary To be agreed
Benefits There is an attractive remuneration and benefits package on offer including car allowance, healthcare and holiday pay.
Duration Rolling Contract
Location North West
Job

Are you looking to move out of the CRO environment and join a pharmaceutical company? If yes, then this is the rôle for you! Our client, a leading blue chip pharmaceutical company with an interest in cardiovasular, diabetes and oncology research, is looking for a CRA to join their North West field team on a long term rolling contract. In this rôle for 50% of you time you will be responsible for the site management of centres in the Cumbria and Lancashire region ensuring that they are ICH GCP compliant. The remaining 50% of the time will be spent in a training co-ordinator capacity, delivering training to CRAs in the field and providing support to more junior CRAs.
This is an excellent opportunity for a junior CRA to take on more responsibility or for a more experienced CRA to move into a senior CRA/training rôle.

Experience

The ideal candidate will have a minimum of 12 months experience covering all aspects of site management (initiation, monitoring and close out) in a range of therapeutic areas (cardiovascular, diabetes or oncology desirable). BSc in a life science or RGN qualification. You will be motivated, enthusiastic and able to work on your own initiative.

 

Job Title CRA/SCRA North East
Salary To be agreed
Benefits There is an attractive remuneration and benefits package on offer including car allowance, healthcare and holiday pay.
Duration Rolling Contract
Location North East
Job

Are you looking to move out of the CRO environment and join a pharmaceutical company? If yes, then this is the rôle for you! Our client, a leading blue chip pharmaceutical company with an interest in cardiovasular, diabetes and oncology research, is looking for a CRA to join their North East field team on a long term rolling contract. In this role for 50% of you time you will be responsible for the site management of centres in the York and Harrogate region ensuring that they are ICH GCP compliant. The remaining 50% of the time will be spent in a training co-ordinator capacity, delivering training to CRAs in the field and providing support to more junior CRAs.
This is an excellent opportunity for a junior CRA to take on more responsibility or for a more experienced CRA to move into a senior CRA/training rôle.

Experience

The ideal candidate will have a minimum of 12 months experience covering all aspects of site management (initiation, monitoring and close out) in a range of therapeutic areas (cardiovascular, diabetes or oncology desirable). BSc in a life science or RGN qualification. You will be motivated, enthusiastic and able to work on your own initiative.

 

Job Title CRA/SCRA
Salary £28,000 basic
Benefits A competitive remuneration package is on offer to the right candidate.
Duration 12 months rolling contract
Location Scotland
Job

Our client, one of the worlds leading pharmaceutical companies, has an urgent requirement for a contract CRA to join their field based team based in Scotland. Initially the contract will be for a period of 12 months, but this will be extended at the end of the term to become an open ended 'rolling' contract. In this rôle you will be responsible for the co-ordination of a large cardiovascular project with centres in and around Scotland. There will also be the opportunity to get involved with diabetes and oncology projects as required, enabling you to gain valuable therapeutic area experience in a pharmaceutical environment. In addition to project responsibilties you will also develop sites in the Scotland region, and this will involve visiting hospitals and reporting on feasibility findings, site evaluation and assessment.

Experience

The ideal candidate will have a minimum of 12 months experience conducting phase II and III cardiovascular projects and monitoring in the field. A BSc in a life science or RGN qualification is preferred.

 


Job Title Clinical Information Administrator
Salary £27,000 p.a. pro rata
Benefits An attractive remuneration package is on offer including holiday pay and healthcare.
Duration The contract will intially be for 6 weeks, full time, to cover long term sick leave, but may be extended to 3 months.
Location Hampshire
Job Our client, a leading pharmaceutical company, has an urgent requirement for an Information Administrator to join their medical information department on a short term contract basis. In this rôle you will be interpreting biomedical data alerts, searching on-line databases and downloading abstract information.
Experience You MUST be familiar with the British Library automated clinical paper ordering process, and have an understanding of copyright law (Private Study Only copy / Copyright Fee Paid copy) to be suitable for this position. Previous experience in a similar rôle is preferred as you will be liasing with the CLA Rapid Clearance System for authorisation to make copies of copyrighted material.

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