Job Opportunities API

Register now • PV Partnership & Operations Manager This job is now closed. PV Partnership & Operations Manager Reference: BBBH28956 Date posted: 30/03/2026 Job details Specialism PVG & Drug Safety Expertise Global Drug Safety Basel, Basel-City, Switzerland Job type Contract Register your interest If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available. Register interest Description Are you ready to lead cutting-edge pharmacovigilance operations that accelerate clinical breakthroughs in biotech? R&D Partners is seeking a PV Partnership and Operations Manager to oversee safety processes and ensure compliance with regulatory requirements for clinical trials and marketed products. You will act as a key expert in pharmacovigilance, collaborating with internal teams, external partners, and vendors to maintain high-quality safety data and operational excellence. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: • Act as the main point of contact for pharmacovigilance activities in partnerships and collaborations. • Provide safety expertise for clinical studies and ensure proper management of safety data. • Lead the development and implementation of Safety Management Plans for clinical trials. • Ensure systems are configured correctly for safety data management in clinical trials and marketed products. • Collaborate with clinical operations, regulatory affairs, and external vendors to ensure smooth data transfer and reporting. • Oversee reconciliation of serious adverse events (SAEs). • Manage safety information for marketed products, including reviewing agreements and materials for compliance. • Lead operational meetings with partners and distributors, ensuring adherence to agreements and quality standards. • Support audits and inspections related to pharmacovigilance partnerships. • Identify and address quality or compliance issues proactively. Key Skills and Requirements: • A degree in biosciences, healthcare, or pharmacy. • Strong understanding of pharmacovigilance regulations for clinical trials and post-marketing, including GVP and ICH guidelines. • Experience in managing safety data, vendor relationships, and pharmacovigilance agreements. • Ability to collaborate effectively with cross-functional teams and external partners. • Attention to detail and problem-solving skills to ensure compliance and quality. For more information, please contact William Tyler. If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page. R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/ Register your interest If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available. Register interest Related jobs Discover our latest opportunities in life sciences and apply now. PSMF Senior Specialist Join a high-impact globalisation project where your PSMF expertise will help strengthen pharmacovigilance compliance across international markets. R&D Partners is seeking a PSMF Senior Specialist to provide expert… Job type: Contract Location: Munich, Bayern, Germany View role Get in touch Have questions or need support? Our team is here to help, contact us to discuss your hiring needs or career goals today.