Scientific Writer III
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The Opportunity
Description
We're looking for a Scientific Writer III, working in Biotechnology/Medical Devices industry in Cambridge, Massachusetts, United States.- Prepares moderately complex clinical documents for one or more programs.
- Coordinates preparation of clinical documents by other writers with minimal supervision.
- Leads document-related meetings, reviews
statistical analysis plans and clinical data reports as needed.
- Mentors junior writers on departmental processes related to document preparation.
- Reviews documents written by junior writers for content and format.
Our Client
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
- BS degree
- 1+ year of regulatory medical writing experience
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?
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