
| City | Cambridge |
| Career Level | Manager / Team Leader |
| Industry | Life Science / Pharmaceutical Industry |
Associate Director, Medical Writing - Cambridge You will be responsible for researching, writing and project managing scientific documents e.g. protocols, final study reports, IMPDs and other regulatory documents covering a wide range of therapeutic areas for clients and regulatory agencies. The role also involves line managing a team of medical writers. A Life Sciences graduate with experience of writing for clinical research and regulatory submissions, you will have a good understanding of full drug development concepts, the ability to interpret medical data, strong PC skills (including Word) and a clear presentation style. For more information or to apply for this position, please send
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