Boyds is looking for a Senior Clinical Research Associate to provide effective management and monitoring of sponsor clinical trials. • Site initiation and routine monitoring through to site close out activities • Feasibility and site selection activities • Performing ethics/IRB submissions • Site contract negotiation and site liaison activities • Being involved in the process of business development and other business activities as require The successful candidate will be/have: • Educated to degree level or equivalent in a scientific field • Proven CRA experience (ideally 5 years) working within a CRO, biotech or pharma company • Strong independent monitoring experience • A very strong understanding of the clinical process across all phases (particularly phase I-IIa) • Full driving licence and a willingness to travel. Contact Sam Whyley-Smith on 01246 580040 or [email protected], quoting ref 50098.