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Senior Safety Scientist

Senior Safety Scientist

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Senior Safety Scientist

  • Location:


  • Sector:


  • Contact:

    Edward Jessel

  • Salary:

    US$75 - US$150 per hour

  • Job type:


  • Contact email:

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  • Published:

    18 days ago

  • Duration:

    6 months

  • Startdate:


Safety (PV) Scientist - Freelance - California
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.

Client are based in California and will offer remote working

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