Principal Scientist, Safety Evaluation & PV Strategy

GSK; Greater London; Hybrid; GBP 90,000 - 130,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

GSK is seeking a SERM Principal Scientist to provide medical/scientific leadership in safety evaluation and risk management across clinical development and post-marketing settings. The role emphasizes PV expertise, cross-functional team leadership, and regulatory documentation support in a hybrid working model at GSK HQ.

You will oversee signal detection, risk mitigation strategies, and governance to protect patient safety while coordinating with global assets and safety surveillance teams.

Qualifications

• Degree in health sciences, pharmacy or a related healthcare discipline.
• Experience in pharmacovigilance, safety evaluation and risk management.
• Familiarity with ICH, GVP and CIOMS guidelines.
• Experience in drug development and regulatory approval processes.

Responsibilities

• Signal detection and evaluation for assigned products.
• Prepare fit-for-purpose safety evaluation documents for internal/regulatory requests.
• Assist in creating RMPs and safety documentation with senior staff.
• Support regulatory reporting and program documents on safety data.
• Ensure inspection readiness and post-audit activities.

Skills

Pharmacovigilance

Safety evaluation

Presentation techniques

Digital fluency

Enterprise leadership

Influencing without authority

Education

Health sciences/pharmacy degree (BSc/MSc/PhD)

Job description

GSK is seeking a SERM Principal Scientist to provide medical/scientific leadership in safety evaluation and risk management across clinical development and post-marketing settings. The role emphasizes PV expertise, cross-functional team leadership, and regulatory documentation support in a hybrid working model at GSK HQ.

You will oversee signal detection, risk mitigation strategies, and governance to protect patient safety while coordinating with global assets and safety surveillance teams.