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Job Description:
In this position you will be responsible for the preparation and review of clinical documents for worldwide submissions to regulatory authorities. Strong knowledge of regulatory documents and templates (eCTD) is required. As a Contract Medical Writer for Bioforce Solutions, you will work for a large NJ-based pharmaceutical company creating documents and templates for Regulatory Submissions projects. You will enjoy a flexible work schedule, competitive compensation, and a comprehensive benefits package.
Responsibilities:
- Prepare CSR's, integrated clinical summaries, safety update reports, overviews, and other regulatory documents on investigational drugs in various stages of clinical development.
- Serve as liaison between outside writing sources and review and edit documents prepared by outside resources.
Qualifications:
- Degree in Life Science related fields with a minimum of a BS is required and MA, PhD or PharmD preferred.
- 5 plus years in Medical Writing, working with regulatory documents (NDA, CSR, eCTD) for a pharmaceutical company or CRO.
About Bioforce Solutions:
Bioforce Solutions is a national workforce solutions firm focused on the Biotech, Pharmaceutical, and Medical Devices industry. Our consultants and candidates work for the best companies on rewarding projects. We value our consultants and candidates highly. During the hiring process we pride ourselves on personal service and responsiveness. Bioforce offers competitive compensation along with a comprehensive benefits package that includes medical insurance, dental insurance, life insurance, short and long term disability, and a matching 401K program.
Contacting Bioforce Solutions:
If you want a representative that cares about your career, call Bioforce Solutions at 888.719.6300 and visit our Website at www.bioforcesolutions.com
Please call for immediate consideration:
Michael Morgan
mmorgan@bioforcesolutions.com
voice: (888)719-6300x1744
Aligning Vision with Ability
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