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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