Within this role you will assume responsibility for the Global Clinical and Scientific management of assigned studies. Your responsibilities will include protocol writing, managing CRO relationships and matrix managing the Global Clinical Trial Team, working alongside the Medical experts.

Suitable candidates will be life science degree educated (or hold a nursing equivalent qualification) and have demonstrable experience in International Trial Management ideally to have included protocol writing and scientific development experience. Experience working previously within the Therapeutic areas highlighted above is highly desirable though not essential and you must be fluent in English.

This is an urgent requirement and immediate consideration will be given to suitable applicants. To apply please send your CV to louis.gicquel@secpharma.com or call + 44 (0) 207 255 6600

For logistical and work permit reasons my client is seeking candidates currently based within the EMEA

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business