Senior Manager, Medical, Regulatory & Pharmacovigilance (Levant)

About the role

As Senior Manager, MRPV for the Levant region (Jordan, Lebanon & Syria), you will act as the strategic link between medical affairs, regulatory compliance and pharmacovigilance, ensuring that products meet the highest safety and efficacy standards across multiple markets.

Key responsibilities

• Lead cross‑functional teams to develop and implement integrated MRPV strategies for product launches and lifecycle management.
• Ensure regulatory compliance across assigned markets while maintaining pharmacovigilance excellence.
• Serve as primary contact for health authorities on medical, regulatory and safety matters.
• Oversee preparation and submission of regulatory dossiers, safety reports and medical information responses.
• Drive continuous improvement of MRPV processes and systems in collaboration with global teams.
• Manage and develop MRPV team members, fostering a culture of quality and compliance.
• Partner with commercial, medical affairs and clinical teams to support business objectives.

Required profile

• Advanced degree in Life Sciences, Pharmacy, Medicine or related field; MD, PharmD or PhD preferred.
• Minimum 7 + years experience in medical affairs, regulatory affairs and/or pharmacovigilance within the pharmaceutical industry.
• Proven track record of leading cross‑functional teams and managing multiple stakeholders across regions.
• Deep understanding of international regulatory requirements (ICH, EMA, FDA and regional authorities).
• Excellent communication and influencing skills with ability to present complex information clearly.
• Fluency in English; additional languages are an advantage.

Required skills