Consultant, Document Management Specialist II, Pharmaceuticals
Summary
Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a Document Management Specialist II to assist with U.S policy and SOP lifecycle document development and management.
Description
Qualifications/Experience
Required:
- Experience with document management and/or project coordination with digital properties such as websites, intranets, and microsites.
- 3 years + of professional experience in a Pharma or other regulated environment.
Preferred:
- Experience working in the MS Teams environment.
- Experience with VeevaVault PromoMats.
- Experience with Tableau/PowerBI reporting and analytics.
Term & Start
Key Responsibilities Due Diligence & Transaction Support Assist with due diligence by reviewing corporate records, contracts, financial documents, and regulatory filings Organize and maintain data rooms, track document requests, and ensure timely responses from...
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