Clinical Trials Assistant / Manager Vacancies

Clinical trials Assistant / Manager Vacancies Clinical trials Assistants and Managers positions typically handled by Seltek. Click the button at the bottom of the page to view our current open positions. Login to view our current vacancies.


This is a clinical trials management position within Europe for a leading CRO and would suit a lead CRA with supervisory experience! This is a field based role and trials managers can be based anywhere in Europe although travel within this region will be required. The trials manager works closely with the project director to deliver studies on time and to budget, taking responsibility for the leadership and training of field based CRAs on assigned projects. All you need to be considered is previous experience in a similar role.


This is your chance to broaden your experience making this a truly exciting career opportunity. This company is rapidly expanding their clinical business with new and exciting trialss, enabling you to link your success with theirs. You will work either directly with top customers or on their outsourced trialss. As such you need to be comfortable with gaining responsibility early on in these challenging roles although you will benefit from excellent ongoing training. As a CRA you will perform all aspects of study site management including routine monitoring and close-out of clinical sites, maintenance of study files, conduct pre-study and initiation visits and liaise with other vendors. At the SCRA level you will assist in managing project budget and investigator site budget, attend project team meetings, plan and attend investigator meetings. You will aslo assist in the preparation/review of protocols, design of case report forms and other study documentation in collaboration with the project manager. You will be rewarded with an excellent benefits package and competitive salary.

What does our client look for? You know who you are. With an appropriate degree level qualification and 12 to 18 months' industry experience, you should have the ability to work/ travel independently and have strong time management and interpersonal skills.


A leading drug development company is looking to appoint a Senior Medical Director to supervise and co-ordinate all activities within the International Medical Affairs Department, and their input into ongoing and new clinical trialss. This is an office based role in the South of the UK although travel will be required internationally. Reporting into the Chief Medical Officer on a global level you will be accountable for the following: departmental/staff management, advising on pre-clinical / clinical development and research ethics, finance/budgets and safety review. In this role you will also have involvement in business development, staff training and client management. An excellent benefits package is available including car/allowance, relocation assistance, pension, private healthcare, life assurance and 25 days holiday. Call now to find out more!

Applications are invited from qualified physicians with FULL GMC REGISTRATION and a broad based clinical background. Candidates must have knowledge of clinical development gained within a pharmaceutical company/CRO background. This is a senior, high profile leadership role within medical affairs and as such candidates must have proven departmental management skills and a dynamic personality.

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