Safety Operations Specialist

Company: BioNTech SE
Apply for the Safety Operations Specialist
Location: London
Job Description:

Safety Operations Specialist

Location: London, United Kingdom

Job ID: 11418

About the Role

As a Safety Operations Specialist, you will play a pivotal role in supporting pharmacovigilance activities across clinical trials and post‑marketing phases. Your contributions will ensure compliance with global safety standards while gaining valuable experience in safety operations. You will work closely with cross‑functional teams to process individual case safety reports (ICSRs), coordinate regulatory submissions, and maintain workflows critical to BioNTech’s mission of advancing healthcare solutions.

Your Contribution

  • Perform and support end‑to‑end case processing activities for clinical trials, including intake, data entry, triage, MedDRA coding, seriousness evaluations, case approval, and safety queries
  • Support case processing for post‑marketing ICSR‑s, including monitoring spontaneous reports and other safety data sources
  • Coordinate case exchanges with partners and track compliance metrics for safety reports through continuous quality control sampling
  • Prepare and conduct quality reviews for SUSAR submissions, DSURs, line listings, and other periodic reports in line with global requirements
  • Execute and maintain workflows such as regulatory reporting, safety inbox screening/intake, data reconciliation, or analytical report generation based on assigned responsibilities
  • Maintain accurate records within the safety database and assist with system testing activities (e.g., user acceptance testing)

A good Match

  • Bachelor’s degree in life sciences, pharmacy, public health or a related field; postgraduate qualification preferred
  • At least 2 years of pharmacovigilance experience in the pharmaceutical/biotech/CRO industry; post‑market setting preferred
  • Minimum 1 year of case processing experience; familiarity with Veeva Vault Safety is ideal
  • Solid knowledge of regulatory requirements (GCP/GVP) across major geographies
  • Strong project management skills combined with cross‑functional collaboration abilities
  • Fluent in written and spoken English

Your Benefits

  • Your flexibility: flexible hours | vacation account
  • Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
  • Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
  • Your health and lifestyle: Company bike
  • Your mobility: Job ticket | Deutschlandticket
  • Your life phases: Employer‑funded pension | Childcare

EEO Statement

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer.

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Posted: May 23rd, 2026