Medical and Promotional Reviewer

3 weeks ago

Cambridge, United States Randstad Life Sciences US Full time

6 Month Contract - Potential to Convert


Cambridge, MA - ideally, 3 days onsite (will consider remote for the perfect candidate)


Must Haves a background in either Virology or Oncology


Job Summary

The Medical and Promotional Reviewer will be a contributing member of the Medical Review Committee (MRC) and the Promotional Material Review Team (PMRT). The Medical and Promotional Reviewer will be responsible for the review and approval of medical and promotional pieces, working closely and collaboratively with other reviewers and stakeholder groups such as medical, legal, and regulatory (MLR), compliance, and commercial teams. This individual will ensure that materials are scientifically and medically accurate, statements are adequately supported and up-to-date, and not misleading. This individual will also verify accuracy of cited data and that content is consistent with current medical opinion according to published literature or guidelines.


Job Responsibilities

  • Conduct comprehensive reviews as the medical reviewer within MRC and PMRT, extending to additional review committees as needed.
  • Provide medical insights and leverage therapeutic medical expertise for MRC, PMRT, and other review committees.
  • Ensure the medical accuracy of a broad spectrum of materials, from disease awareness and pipeline communications to marketing and internal documents.
  • Support cross-functional collaboration; help align US and Global Medical Affairs projects as needed.
  • Enhance the MRC framework by offering expertise, conducting training sessions, and managing vendor relations as needed.
  • Maintain a high knowledge of emerging data and developments across all therapeutic areas, proactively shaping the medical and scientific discourse of our products.


Education & Qualifications

Required

  • PhD/PharmD required
  • 3+ years of job relevant experience in a Medical or Promotional Materials Review Committee
  • Experience working in Veeva Vault
  • Experience working in Medical Affairs in the biotechnology or pharmaceutical industry
  • Experience and knowledge of FDA, EU, ICH guidelines and regulations.

Preferred

  • Prior experience in infectious diseases and/or vaccines is preferred
  • Proven ability to effectively manage interactions with internal and external agency partners.
  • Ability to interact with cross-functional teams in a matrixed organization.
  • Well-organized self-starter, hard-working and independent.
  • Strong ability to manage time effectively and prioritize tasks to meet deadlines
  • Strong negotiation, verbal/written communication, and interpersonal skills with a good awareness of global cultural differences.
  • Excellent attention to detail.
  • Strong written and verbal communication skills.

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