Job Description

At our client’s organization, where passion meets potential, we believe in fostering a culture of continuous learning and growth. If you're driven by excellence and eager to be part of a dynamic and innovative team, join us in making a lasting impact on the pharmaceutical industry.

We are seeking an experienced RA/PV Manager to lead our Regulatory Affairs and Pharmacovigilance (RA/PV) projects. This key leadership role involves overseeing the execution and delivery of all RA/PV projects, performing quality checks on team output, and managing all regulatory submissions and pharmacovigilance reporting for multiple markets.

Key Responsibilities:

• Lead RA/PV projects from initiation to completion, ensuring timely and accurate delivery.
• Draft and compile dossiers for various global markets.
• Perform quality checks on all RA/PV team outputs.
• Manage regulatory submissions and pharmacovigilance reporting for the team.
• Ensure compliance with regulatory authorities across multiple markets.

Requirements:

• Education: Master’s Degree in Life Sciences, Health, or Biomedical
• Sciences.
• Experience: 10 to 15 years of experience in Regulatory Affairs and
• Pharmacovigilance (RA/PV) within regulated markets.

Skills:

• Extensive experience across multiple markets, with a deep understanding of regulatory and pharmacovigilance processes.
• Excellent written and verbal English communication skills.
• Proven experience managing and mentoring teams.
• Strong familiarity with submissions to competent authorities.

Why Join Us?

• Lead a talented team within a globally recognized organization at the forefront of pharmaceutical innovation.
• Shape the future of regulatory and pharmacovigilance practices while working in a highly collaborative and fast-paced environment.
• Seize opportunities for professional growth and leadership development in a challenging, rewarding role.

Take the next step in your leadership journey—apply today and lead the way in transforming healthcare!

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