Senior Pharmacovigilance & Safety Director

Senior Pharmacovigilance & Safety Director

Full-Time 80000 - 100000 Β£ / year (est.) No working from home possible
Meeveem Limited

At a Glance

  • Tasks: Lead safety evaluation and risk management for global assets in pharmacovigilance.
  • Company: Join GSK, a leader in healthcare innovation and patient safety.
  • Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
  • Other info: Dynamic role with significant impact on clinical development and post-marketing safety.
  • Why this job: Make a real difference in patient safety and collaborate with cross-functional teams.
  • Qualifications: 5+ years in pharmacovigilance and strong data interpretation skills required.

The predicted salary is between 80000 - 100000 Β£ per year.

GSK is seeking a Pharmacovigilance professional to support safety evaluation and risk management for a portfolio of global assets.

The role focuses on leading PV strategy, governance, and cross-functional collaboration to ensure patient safety across clinical development and post-marketing settings.

The ideal candidate has 5+ years in pharmacovigilance, strong data interpretation skills, and experience with regulatory interactions.

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Senior Pharmacovigilance & Safety Director employer: Meeveem Limited

Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.

Meeveem Limited

Contact Details:

Meeveem Limited Recruitment Team

We think you need these skills to ace Senior Pharmacovigilance & Safety Director

Pharmacovigilance
Safety Evaluation
Risk Management
Data Interpretation
Regulatory Interactions
Cross-Functional Collaboration
Clinical Development