Greenkey Resources
Published
June 16, 2020
Location
Remote, United States of America
Category
Other  
Job Type
Work Setting
Remote / Home-based

Description

Duties

  • Ensure medical/scientific statements in promotional, educational, and medical affairs-based materials are supported by appropriate, up to date, references.
  • Candidate will also ensure that all materials associated with currently marketed agents are consistent with the approved FDA label
  • Candidate will ensure that all tables and graphs are populated with correct data/numbers/statistics
  • Upon completion of review, final MLR/PRC signoff will be made by designated medical affairs team members
  • Attend MLR/PRC meetings as needed
  • Partner with Commercial and vendors as needed
  • Participate in Launch meetings where needed
  • Work 20-30 hours depending on activity

Qualifications

Required

  • MD, Ph.D., or PharmD (terminal degree)
  • 3-5 years’ experience in pharmaceutical MLR/PRC review processes particularly as it relates to hematological and solid tumors.
  • Oncology experience
Apply
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