Company Overview:
Jazz Pharmaceuticals plc is a global biopharmaceutical company that develops life-changing medicines for people with serious diseases. We are committed to innovation and excellence in all aspects of our business. As a Senior Medical Safety Lead, you will be part of our talented team working to develop new treatments and improve patient outcomes.
The role offers a competitive salary package of $125,000 - $155,000 per annum, depending on location and experience. You will also have access to various benefits, including health insurance, retirement savings plan, and flexible paid vacation.
About the Job: We are seeking an experienced Senior Medical Safety Lead to join our Global Drug Safety & Pharmacovigilance department. The successful candidate will have at least 5 years of experience in pharmacovigilance, including 3 years in surveillance and/or risk management functions. They will be responsible for leading the coordination of aggregate safety reports and providing high-level scientific expertise in safety evaluation and risk management.
Responsibilities:
Lead the production of safety-related documents, including signal evaluation reports and periodic benefit-risk evaluations. Collaborate with medical experts to identify and prioritize safety concerns. Develop and implement risk management strategies to minimize the risk of adverse events associated with our products. Liaise with cross-functional teams to ensure timely and accurate submission of safety information to regulatory authorities.
The role offers a competitive salary package of $125,000 - $155,000 per annum, depending on location and experience. You will also have access to various benefits, including health insurance, retirement savings plan, and flexible paid vacation.
About the Job: We are seeking an experienced Senior Medical Safety Lead to join our Global Drug Safety & Pharmacovigilance department. The successful candidate will have at least 5 years of experience in pharmacovigilance, including 3 years in surveillance and/or risk management functions. They will be responsible for leading the coordination of aggregate safety reports and providing high-level scientific expertise in safety evaluation and risk management.
Responsibilities:
Lead the production of safety-related documents, including signal evaluation reports and periodic benefit-risk evaluations. Collaborate with medical experts to identify and prioritize safety concerns. Develop and implement risk management strategies to minimize the risk of adverse events associated with our products. Liaise with cross-functional teams to ensure timely and accurate submission of safety information to regulatory authorities.
