| Description: | Are you an experienced Senior CRA looking for a route into study management? Interested in working for a blue chip biopharma company? If the answer is yes to these questions read on! We are working with a leading, blue chip biopharma company based in West London who urgently need an experienced Lead CRA to take charge of European clinical and local study management activities across several general medicine projects in either phase II/III or phase III/IV. This is a contract position for 11 months with the possibility for further extension or conversion into a permanent contract. In this role you will work closely with study managers to deliver European studies in nephrology. Essentially you will manage all start up activities through liaison with CROs, conduct feasibility assessments, co-ordinate ethics applications and support CRAs in the field with protocol related queries. You will also manage the clinical budget and timelines making sure that the clinical deliverable is achieved within set timelines. Who are we looking for? You must have experience of co-ordinating clinical activities across several countries, with a strong background in feasibility and start up. Previous experience in nephrology or general medicine is an advantage. This contract is available on a full time basis through Seltek Consultants - competitive rates of pay are on offer for limited company contractors and competitive salaries and benefits for candidates interested in working through Seltek on a contract for services. Call now for more details! |
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