Sr Manager, Global Case Management, Safety and Benefit-Risk Management

Biogen Idec uses cutting edge science to discover, develop, manufacture and market biological medicine for the treatment of serious diseases with high unmet need. We are the world's oldest independent biotechnology company and a Fortune 500 company with more than $4 billion in revenues and offices located worldwide.

We are the trusted source of vital therapies for multiple sclerosis, such as AVONEX and TYSABRI. We also discovered RITUXAN, the world's most prescribed treatment for non-Hodgkin's lymphoma and an effective treatment for rheumatoid arthritis. Patients worldwide benefit from our products, and count on us not only for their medication, but also for a variety of support programs.

In addition to our global leadership in the treatment of MS, we have leveraged our R&D and commercial expertise to pursue life-saving and life-changing therapies for other neurodegerative diseases, including ALS (Lou Gehrigs disease), Alzheimers and Parkinsons diseases. We are continuing to advance our high potential programs in hemophilia and build on our scientific strength in immunobiology.

Our culture of excellence empowers employees to challenge conventional wisdom and propose better ways of doing thing; bringing additional value to all of our stakeholders, starting with the people we come to work for everyday - the patients, our families and ourselves.

Responsible for managing the daily activities of the clinical trial Safety and Benefit-Risk Management function including the direct supervision of Safety Associates in the collection, evaluation, and collation of both clinical trial and postmarketing adverse event reports.
- 5+ years in a clinical setting
- 7+ years in Drug Safety department in pharmaceutical/biopharmaceutical industry.
- Supervisory/ direct line management required

Minimum of Bachelor's level degree in nursing, pharmacy, or other health related profession.