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Regulatory Senior Associate/Associate Manager

EPM Scientific Newark, CA

  • Expired: over a month ago. Applications are no longer accepted.
Job Description

A clinical-stage company located in the San Francisco Bay Area is looking for a Regulatory Affairs Manager/Senior Regulatory Associate to support their clinical development projects. This role is a 6-month contract-to-hire opportunity.

Responsibilities:

  • Prepare and compile submissions
  • Act as a regulatory representative for assigned clinical studies
  • Mange regulatory document preparation and timelines
  • Support clinical trial application activities
  • Coordinates the authoring, review, and approval of Clinical, and Nonclinical documents

Requirements:

  • BA/BS in scientific or related field
  • 4+ years pharmaceutical industry experience in regulatory affairs position
  • 1-year clinical regulatory experience required
  • Strong understanding of international pharmaceutical guidance and drug development processes

If interested in the Regulatory Affairs Manager/ Senior Regulatory Associate position, don't hesitate apply now!

EPM Scientific

Address

Newark, CA
USA

Industry

Government

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