FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmacovigilance, risk management, and safety evaluation within oncology clinical development, with strong capabilities in data analysis and regulatory submissions. Proven ability to lead cross-functional teams and communicate effectively with stakeholders and regulatory authorities.
Highest-signal resume keywords
Medical Degree With GMC RegistrationPharmacovigilance ExperienceSignal Detection And EvaluationClinical Development UnderstandingRegulatory Submission Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Risk ManagementSafety EvaluationData AnalysisClinical JudgementSignal DetectionEpidemiology KnowledgeBiostatistics KnowledgePost-Marketing Safety ProcessesSafety Review Team LeadershipRegulatory Document Preparation
Soft Skills
Excellent Communication SkillsCoaching And MentoringCollaborationRelationship BuildingEvidence-Based Decision Making
Certifications & Qualifications
Postgraduate Clinical TrainingSpecialisation In Clinical Discipline
Industry Keywords
Oncology AssetsClinical TrialsSafety SignalsGlobal Regulatory SubmissionsCross-Functional TeamsSafety Review TeamsSERM ActivitiesOperational EffectivenessGovernance ProcessesExternal Safety Forums
About the role
Key responsibilities & impact- Provide medical and scientific leadership in safety evaluation and risk management of GSK oncology assets in clinical development
- Lead pharmacovigilance and risk management activities for assigned oncology assets and clinical trials
- Define and drive strategy for evaluating and managing 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 safety components of global regulatory submissions
- Apply clinical judgement to complex and conflicting data to inform benefit–risk decisions
- Escalate safety concerns in line with governance processes
- Represent Safety on cross-functional Clinical Matrix and Project Teams
- Lead cross-functional teams addressing urgent and complex product safety issues
- Contribute to or lead Safety Review Teams
- Build collaborative relationships across functions and geographies
- Coach and mentor colleagues and contribute to capability development
- Communicate and align with Safety Leads, senior SERM leadership, and stakeholders
- Present safety issues and recommendations to senior governance committees
- Represent GSK with regulatory authorities, external experts, and partners
- Contribute to safety strategy for clinical programmes and broader SERM activities
- Identify process improvements, drive innovation, and enhance operational effectiveness
Requirements
What you’ll need- Medical degree with current GMC registration or eligibility to practise in the UK and relevant clinical experience
- Completion of formal postgraduate clinical training, such as residency or specialty training
- Significant experience in pharmacovigilance, drug safety, or medical affairs
- 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 ability to deliver clear, evidence-based recommendations
- Postgraduate specialisation in a clinical discipline or pharmaceutical medicine preferred
- Experience contributing to regulatory submissions and periodic safety reports preferred
- Knowledge of epidemiology, biostatistics, or real-world evidence relevant to safety assessment preferred
- Experience leading Safety Review Teams or acting as safety lead for major programmes preferred
- Prior engagement with regulatory authorities and external safety forums preferred
- Demonstrated ability to coach and develop colleagues in medical, scientific, or safety roles preferred
Benefits
Comp & perks- Annual bonus
- Eligibility to participate in share-based long-term incentive program
- Health care and other insurance benefits for employee and family
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave
- Remote working support
- Reasonable adjustments and application/interview support