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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in pharmacovigilance, focusing on safety evaluation and risk management throughout clinical development and post-marketing phases. Proficient in preparing regulatory documents and safety evaluations while ensuring compliance with international guidelines.
Highest-signal resume keywords
PharmacovigilanceSafety EvaluationRisk ManagementScientific WritingRegulatory Reporting
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Safety Data EvaluationRisk Reduction StrategiesClinical Protocol DesignRegulatory ComplianceAttention to Detail
Soft Skills
Clear CommunicationMentoringCollaborationCross-Functional Teamwork
Tools & Technologies
Safety DatabasesData Visualization Tools
Certifications & Qualifications
Health Sciences DegreeHealthcare Professional Qualification
Industry Keywords
International Pharmacovigilance GuidelinesDrug Development ProcessesPost-Marketing Safety OversightSafety GovernanceRegulatory Inspections
About the role
Key responsibilities & impact- Lead or contribute signal detection and evaluation activities for assigned products, applying strong scientific judgment
- Prepare and review global regulatory reports and risk management plans, ensuring accuracy and timely delivery
- Support safety governance meetings and collaborative safety review teams for clinical and post-marketing safety oversight
- Contribute to the design and implementation of risk-reduction strategies in clinical protocols and product information
- Build and maintain effective relationships across teams, providing clear communication and mentoring colleagues where appropriate
- Participate in process improvements to enhance compliance, quality, and efficiency within safety evaluation activities
- Support patient safety across products in clinical development and post-marketing settings
- Evaluate safety data and manage risks across key products
Requirements
What you’ll need- A degree in Health Sciences or Healthcare Professional qualification (for example, BSc, MSc, PhD, RN, NP, PharmD)
- Practical experience in pharmacovigilance focusing on safety evaluation and risk management during clinical development and post-marketing phases
- Understanding of international pharmacovigilance guidelines and drug development and approval processes
- Experience working effectively in cross-functional, matrix teams
- Strong scientific writing skills with the ability to prepare detailed safety evaluations and regulatory documents
- Ability to manage multiple tasks with attention to detail and deliver high-quality results on time
- Advanced degree (e.g., PhD, MD, or equivalent) is a plus
- Previous experience working in large, global pharmaceutical organizations is a plus
- Familiarity with early clinical development safety activities is a plus
- Experience contributing to safety governance and regulatory inspections or audits is a plus
- Knowledge of relevant safety databases and data visualisation tools is a plus
- Comfortable working in a hybrid model that combines remote and on-site work is a plus
Benefits
Comp & perks- Annual bonus may be offered
- Eligibility to participate in a share-based long-term incentive program may be offered
- Hybrid working model with flexible working between home and UK offices
- Agile working culture and flexibility
- Adjustments to the recruitment process for candidates who require them