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Key Responsibilities:

  • Conduct scientific review and evaluation of ICSRs and clinical trial SAEs.
  • Prepare high quality case narratives and support regulatory ready ICSR submissions.
  • Perform ongoing safety surveillance through analysis of adverse event data.

Qualifications:

  • RN or bachelor’s degree in health sciences or related field required.
  • 5+ years of experience in drug safety.
  • Working knowledge of global PV regulations and guidelines.

Compensation:

  • Eligible for a discretionary annual bonus.
  • Participation in our equity program.
  • Comprehensive benefits package.

Centessa Pharmaceuticals

Centessa Pharmaceuticals is a new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. They are advancing a portfolio of high conviction programs with strong biological validation and their asset-centric model offers a unique R&D logic.

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