Oncology Pharmacovigilance Director

GSK; North East; Hybrid; GBP 127,000 - 212,000; Full time

Benefits offered by this job

Annual bonus

Health care and other insurance

Retirement benefits

Paid holidays

Vacation

Paid caregiver/parental and medical-le

Job summary

GSK invites applications for a role that drives pharmacovigilance strategy and risk management across products in clinical development and post- marketing settings. You will lead safety governance, collaborate with cross‑functional teams, and interact with regulators to ensure compliant safety practices.

The role emphasizes strong analytical evaluation, issue escalation, and development of safety strategies with global impact. Hybrid work arrangement within the United States is offered.

Qualifications

• PhD/PhD for Scientist (preferred) or Bachelors of Science in Life Sciences or Medical Sciences (minimum standard)
• Advanced experience (5+ years) in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety
• Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management, encompassing both clinical development and post‑marketing activities
• Experience with Signal Detection and safety surveillance
• Knowledge/experience of international pharmacovigilance requirements (e.g., ICH, GVP modules, CIOMS initiatives) and drug development and approval processes.

Responsibilities

• Leads Pharmacovigilance and Risk Management Planning and develops strategy for evaluation of issues in the clinical matrix.
• Leads the safety component of global regulatory submissions.
• Demonstrates strong evaluation and analytical skills for literature review and data synthesis.
• Ensures risk‑mitigation strategies are implemented; escalates safety issues as needed.
• Leads safety governance in cross-functional teams across clinical development and post‑marketing settings.

Skills

Digital Fluency

Enterprise Leadership

Influencing Without Authority

Pharmacovigilance

Presentation Techniques

Education

PhD/PhD for Scientist (preferred)

Bachelors of Science in Life Sciences or Medical Sciences

Job description

GSK invites applications for a role that drives pharmacovigilance strategy and risk management across products in clinical development and post- marketing settings. You will lead safety governance, collaborate with cross‑functional teams, and interact with regulators to ensure compliant safety practices.

The role emphasizes strong analytical evaluation, issue escalation, and development of safety strategies with global impact. Hybrid work arrangement within the United States is offered.