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Senior Associate II, Postmarketing Drug Safety and Risk Management - Biogen Idec
Sep 22
Location: Cambridge, MACategories: All Categories
Website: http://posttrak.arbita.net/cgi-bin/PostTrak.cgi?RefCode=R9474282206549
Position Description
Responsible for the receipt, evaluation, classification, processing and follow-up of postmarketing adverse event reports.
Responsible for processing adverse events in compliance with internal Procedures and US and Health Canada regulations. Duties include classification of events, determining follow-up requirement, writing case narratives, reporting per regulations, and closing cases. Also responsible for other ad hoc tasks and activities as required by management.
Qualifications:
Pharmacy, nursing, or other health care related profession. Experience in clinical setting and/or pharmaceutical or biotechnology industry.
About Biogen Idec: Transforming Discovery into Care
With operations across the Americas, Europe, and Asia, Biogen Idec (NASDAQ:BIIB) is one of the world’s leading biotechnology companies, creating new standards of care in oncology, neurology, and immunology. Every day, employees of Biogen Idec make a difference in people’s lives, through pioneering research and development, manufacturing, and our worldwide commercial capabilities.
Learn more at www.biogenidec.com/careers.
Biogen Idec is proud to be an equal opportunity employer
