Senior Clinical Trial Specialist - Oncology - East Anglia - £Neg

Move into a junior project co-ordination role with no monitoring! When you work for this leading biopharmaceutical company you work for an innovative and progressive organisation committed to bringing novel biological products to market for the treatment of cancer, renal diseases and inflammatory or immunological conditions. This company has an impressive pipeline of new drugs in clinical development and its an exciting time to become part of the study management team! Working from the company offices in Cambridge you will be part of the oncology therapeutics team, supporting study managers with the planning and implementation of European phase II-III studies. Your remit will include developing protocols and study documents, identifying investigators, developing recruitment strategies, drug supply management, start up activities, budget tracking and general local project management activities. Studies are run through CROs and other vendors, and it will be your job to work closely with these providers throughout the course of the study providing support and direction where needed. The role is available on an 11 month contract with the possibility of extension or conversion to a permanent position. This is an excellent opportunity for CRAs to move into a project co-ordination role with no monitoring required! Who should apply? The ideal candidate will have a scientific background with a proven track record in clinical development as a CRA. Exposure to phase II-III clinical trials in oncology is essential. Experience of dealing with external vendors, budget administration and site selection activities is desirable. Call Diane now on 01753 832762 / 07812 180025 for more information on how you can fast track your career into project management!