
| City | Cambridge |
| Career Level | Senior Specialist / Project Manager |
| Industry | Life Science / Pharmaceutical Industry |
Associate Medical Director - Cambridge Key areas of responsibility include providing project-specific clinical research medical services and medical support for pharmacovigilance and medical information services. You will help plan, prepare and review/approve regulatory submissions, protocols, Investigator Brochures, among other documents. In addition you will provide a specialist medical advisory service, assist in medical/safety training and will have the opportunity to develop skills in Pharmaceutical medicine including Specialist Therapeutic areas. You will be GMC registered. Specialist or general post-registration clinical practice experience is required, preferably with some exposure
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