Clinical Trial/Medical Affairs Consultant

  • Foster City, CA
  • Posted 8 hours ago | Updated 4 hours ago

Overview

Hybrid
$40 - $60
Contract - W2
Contract - 12 Month(s)

Skills

clinical
medical
medicine
health

Job Details

Our direct BioPharmaceutical client, is looking to hire a Clinical Trial/Medical Affairs Consultant - Hybrid at Foster City, CA (2 days onsite).
Specific Job Requirements:
  • Demonstrate deep subject matter expertise with regard to LIVE products as well as client's pipeline and competitive products.
  • Prepare presentation materials for internal and external meetings, including Advisory Boards.
  • Serve as an information resource and trainer to client's colleagues, including the Medical Scientists, including medical educational activities, grants and investigator-sponsored/collaborative studies.
  • Support data generation activities through:
    • Critical review of global ISRs, Ph 3b and P study proposals
    • Manage HBV Phase IV portfolio as a Global Project Manager, including liaising with key cross-functional partners such as clinical operations and local affiliate
    • Review abstracts and/or manuscripts that result from the phase IV program
    • Support the management and documentation of phase IV study status.
  • Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications.
  • Provide medical and scientific coverage and support at key scientific meetings.
  • Support project leads in the execution and tracking of their projects (eg. Global Medical Affairs Plan of Action, publications, reviews of medical and commercial assets, etc.).
  • Oversee medical and scientific review of promotional materials for GRC and MRC.
  • Support tracking of purchase orders, budget tracking and invoicing for the viral hepatitis franchise.
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