Global Pharmacovigilance Excellence Lead
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Job Description
Global Pharmacovigilance Excellence Lead overseeing safety and efficacy of clinical trials for new medicines. Responsible for leading transformational projects and ensuring compliance in GPV activities.
Responsibilities:
- Oversee pharmacovigilance and drug safety operations, balancing quality, timelines, and stakeholder expectations.
- Develop plans for capability-building projects, including project plans and business cases.
- Develop and communicate project plans and milestone achievements to key stakeholders and governance committees.
- Support updates of procedures, tools, data flows and documentation for GPV activities.
- Partner with IT to evolve relevant systems, such as automation, workflow optimisation, and responsible AI integration.
Requirements:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Significant experience in pharmacovigilance or drug safety, ideally within the clinical research or pharmaceutical industries.
- Strong understanding of regulatory requirements related to drug safety and reporting.
- Excellent analytical and problem-solving skills, with a focus on data-driven decision-making.
- Strong communication and interpersonal skills, capable of engaging and influencing diverse stakeholders.
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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