Benefit Risk Scientist

UCBRaleigh, NC
11d$124,000 - $163,000Hybrid

About The Position

We are looking for a Benefit Risk Scientist who is analytical, collaborative, and detail-oriented to join us in our Patient Benefit Risk and Medical Safety team , based in our Raleigh, North Carolina office. About the role You will contribute to the evaluation, interpretation, and communication of benefit-risk insights across several medicines at different stages of development. You will support the creation of safety and benefit-risk strategies, contribute to scientific documentation, and ensure high‑quality analyses aligned with regulatory requirements. Who you'll work with You will be working in a team that collaborates closely with medical, clinical, statistical, and regulatory colleagues. You will partner with Benefit Risk Leads and cross-functional teams to monitor and communicate the benefit-risk profile of each medicine.

Requirements

  • Bachelor's degree
  • Minimum 2 years' experience in the biopharmaceutical industry with exposure to safety evaluation or benefit-risk assessment.
  • Strong scientific writing skills with the ability to learn different systems quickly.
  • Ability to analyze complex data and communicate findings clearly.
  • Strong organizational skills with the ability to work on multiple projects.
  • Excellent written and verbal communication skills in English.
  • Ability to adapt in dynamic environments and apply sound judgement.

Nice To Haves

  • Advanced degree in a scientific field (MD, PharmD, PhD).
  • Demonstrable experience in supporting multiple safety-related outputs and working knowledge of the international regulations governing drug safety.

Responsibilities

  • Analyze and interpret data from multiple sources to identify and assess potential new risks and incorporate findings into benefit-risk plans.
  • Support the implementation of safety monitoring and risk management strategies in clinical development programs.
  • Prepare and contribute to high‑quality benefit-risk and safety documentation for regulatory submissions.
  • Ensure scientific accuracy, clarity, and compliance in all written deliverables.
  • Collaborate with stakeholders to ensure timely escalation and alignment on safety topics.
  • Stay current on scientific and regulatory developments relevant to benefit-risk assessment.
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