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Safety (PV) Scientist - Freelance

Safety (PV) Scientist - Freelance

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Safety (PV) Scientist - Freelance

  • Location:

    United States of America

  • Sector:

    Pharma, Pharmacovigilance - Pharma

  • Contact:

    Edward Jessel

  • Salary:

    Negotiable

  • Job type:

    Interim/Contract

  • Contact email:

    pharmajobs@msigroupltd.com

  • Job ref:

    EJ-SPVS_1637840326

  • Published:

    12 days ago

MSI Pharma is working with a global biopharma to source a Safety Writing Scientist to support the Global Patient Safety Unit for an initial 6 month freelance contract.

The role:

  • As the Safety Scientist, you will be writing benefit-risk assessments, safety risk management strategies, safety signal assessments, regulatory submissions, aggregate reports, and publications.
  • You will lead the preparation of Patient Safety deliverables, including planning, contributing to analysis strategy, writing, presentation as well as review and approval of documents and deliverables in scope: DSUR, SMR, PBRER /PSUR, SSAR, SOV, RMP, PAER, SRM Strategy document, regulatory responses, submission documents, relevant and other regulatory and safety annual reports.
  • You will provide mentorship to relevant vendors and oversee the work, ensuring the final deliverables meet quality guidelines.
  • Perform literature review and summary of literature for AR, RMP, epidemiology, product renewals, safety evaluations
  • Assure quality and consistency across Patient Safety deliverables, including compliance with regulatory requirements and compliant with agreed and defined timelines.
  • Present analysed relevant adverse event/scientific/clinical/epidemiological data to a variety of audiences
  • Collaborate in the planning, preparation, and review of epidemiologic/scientific manuscripts, abstracts, posters, etc for submission to scientific journals/conferences including generation of lay language summaries for patients as necessary.

You should have:

  • Bachelor's Science degree or the equivalent is an absolute must
  • As is extensive experience in pharmacovigilance, medical writing, including working with vendors, clinical safety or clinical development
  • A good understanding of applicable regulations in pharmacovigilance and clinical development
  • Have the ability to project manage deliverables in a matrix environment with competing priorities