Sr. Clinical Documentation Specialist at Alkermes, Inc. in Waltham, Massachusetts

Job Description:

Alkermes is seeking a highly organized and experienced Clinical Documentation Specialist to support the Clinical Operations department as the primary person responsible for supporting the Clinical Study Team (CST) with trial document management, conducting Quality Control checks (QC), and filing of documentation in the Veeva electronic Trial Master File (eTMF). This position will work closely with CST Functional Area Leads (FALs) and the Clinical Quality team.

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