Clinical Research Associate - £23k

An excellent opportunity to gain monitoring experience within clinical pharmacology! Take responsibility for managing UK sites participating in domestic and international phase I-III trials. The Company: A small, speciality CRO with global reach! Working closely with collaborators and other small service providers this company can support local and global clinical studies or development programmes for pharmaceutical and medical device products from concept through to phase IV. Established in 1987 in Germany this company now has offices in the UK, Israel, Benelux, Spain, Italy, Austria, France, USA and Japan. This is a people focused company who believe in rewarding hard work and enthusiasm. You will have the opportunity to progress quickly into a more senior role if you can demonstrate the ability to do so. The Job: This is a full site management role and you will be responsible for feasibility, site selection, initiation, routine monitoring and close out of hospital and GP sites in the UK. This is an office based position in East Anglia although you will be expected to travel approx 50% of the time. Working on phase I-III studies you will gain exposure to a range of therapy areas and indications including oncology, infectious disease and internal medicine - all high profile research areas! The Person: To fit in with the existing team you will be enthusiastic, dynamic and a real team player. Educated to degree level you will already have 12 months monitoring experience and be looking for the opportunity to take on more site management responsibility. You must be flexible regarding travel and willing to go the extra mile! If you are looking for the opportunity to progress to SCRA level quickly this is the company for you!
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