Medical Director

Meeveem Limited; Greater London; On-site; GBP 110,000 - 150,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

GSK is seeking a medical lead in pharmacovigilance to supervise safety evaluation and risk management for oncology assets in clinical development. The role focuses on interpreting safety data, identifying signals, and delivering evidence-based recommendations to support benefit–risk decisions.

You will contribute to global governance, lead cross-functional teams, and mentor colleagues while engaging with regulators and external experts to shape the safety profile of innovative oncology medicines.

Qualifications

• Significant experience in pharmacovigilance, drug safety, or medical affairs.
• Demonstrated expertise in signal detection, evaluation, and risk management.
• Strong understanding of clinical development and post-marketing safety processes.
• Excellent written and verbal communication skills, including preparation of medical and regulatory documents.

Responsibilities

• Lead pharmacovigilance and risk management activities for oncology assets and clinical trials.
• Define and drive strategy for evaluation and management of safety issues across development lifecycle.
• Analyse and interpret clinical data, literature, and evidence to identify safety signals.
• Provide expert medical input into safety components of regulatory submissions.
• Escalate safety concerns in line with governance processes.
• Represent Safety on cross-functional teams and lead safety review activities.

Skills

Pharmacovigilance

Clinical development

Signal detection

Risk management

GMC registration

Cross-functional leadership

Communication

Education

Medical degree

Job description

Position Summary

Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development.

Responsible for the interpretation of safety data, identification and escalation of safety signals, and delivery of clear, evidence-based recommendations to support benefit–risk decisions. This role contributes to global governance and plays a critical part in protecting patient safety and shaping the safety profile of innovative oncology medicines.

Key Responsibilities

Scientific / Medical & Pharmacovigilance Expertise

• Lead pharmacovigilance and risk management activities for assigned oncology assets and clinical trials
• Define and drive strategy for the evaluation and management of safety issues across the clinical development lifecycle
• Analyse and interpret clinical data, literature, and emerging evidence to identify and assess safety signals
• Provide expert medical input into the safety components of global regulatory submissions
• Apply sound clinical judgement to complex and sometimes conflicting data sets to inform benefit–risk decisions
• Ensure timely escalation of safety concerns in line with governance processes

Matrix Leadership & Cross-functional Collaboration

• Represent Safety on cross-functional Clinical Matrix and Project Teams
• Lead cross-functional teams to address urgent and complex product safety issues
• Actively contribute to and, where appropriate, lead Safety Review Teams (SRTs)
• Build strong, collaborative relationships across functions and geographies
• Coach and mentor colleagues, contributing to capability development within the organisation
• Ensure effective communication and alignment with Safety Leads, senior SERM leadership, and key stakeholders

Communication, Influence & Governance

• Lead presentations on safety issues and recommendations to senior governance committees
• Influence decision-making through clear, credible, and evidence-based communication
• Represent GSK in interactions with regulatory authorities, external experts, and partners
• Contribute to the development of safety strategy for clinical programmes and broader SERM activities
• Identify opportunities to improve processes, drive innovation, and enhance operational effectiveness
• Operate with strong awareness of the internal and external regulatory and scientific environment

Why Join Us?

This is an opportunity to play a pivotal role in advancing GSK’s oncology pipeline, with direct impact on patient safety and global health outcomes.

You will:

• Shape the safety strategy of innovative oncology medicines
• Engage with senior governance and influence key development decisions
• Work within a highly collaborative, global matrix environment
• Contribute to scientific excellence and continuous improvement in safety science

Basic Qualifications

• Medical degree with current GMC registration (or eligibility to practise in the UK) and relevant clinical experience
• Completion of formal postgraduate clinical training (e.g., residency or specialty training)
• Significant experience in pharmacovigilance, drug safety, or medical affairs
• Demonstrated expertise in signal detection, evaluation, and risk management
• Strong understanding of clinical development and post-marketing safety processes
• Experience working effectively in matrixed, cross-functional environments
• Excellent written and verbal communication skills, including preparation of medical and regulatory documents
• Strong clinical judgement and the ability to deliver clear, evidence-based recommendations

Preferred Qualifications

• Postgraduate specialisation in a clinical discipline or pharmaceutical medicine
• Experience contributing to regulatory submissions and periodic safety reports
• Knowledge of epidemiology, biostatistics, or real-world evidence relevant to safety assessment
• Experience leading Safety Review Teams or acting as safety lead for major programmes
• Prior engagement with regulatory authorities and external safety forums
• Demonstrated ability to coach and develop colleagues in medical, scientific, or safety roles

Working Model

This role is hybrid, based in the United Kingdom. You will be expected on site for key meetings, governance activities and team collaboration. Remote working is supported to balance focused work and stakeholder engagement.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.