Job Overview:
Jazz Pharmaceuticals plc is a global biopharmaceutical company dedicated to developing life-changing medicines for people with serious diseases. 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. The estimated salary for this role is $120,000 - $150,000 per annum, depending on location and experience.
About Us: Jazz Pharmaceuticals plc is a global leader in oncology and hematology. Our purpose is to innovate to transform the lives of patients and their families. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology.
Key Responsibilities:
Liaise with cross-functional teams to ensure timely and accurate submission of safety information to regulatory authorities. Develop and implement risk management strategies to minimize the risk of adverse events associated with our products. Provide medical writing support for safety-related documents, including signal evaluation reports and periodic benefit-risk evaluations. Collaborate with medical experts to identify and prioritize safety concerns.
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. The estimated salary for this role is $120,000 - $150,000 per annum, depending on location and experience.
About Us: Jazz Pharmaceuticals plc is a global leader in oncology and hematology. Our purpose is to innovate to transform the lives of patients and their families. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology.
Key Responsibilities:
Liaise with cross-functional teams to ensure timely and accurate submission of safety information to regulatory authorities. Develop and implement risk management strategies to minimize the risk of adverse events associated with our products. Provide medical writing support for safety-related documents, including signal evaluation reports and periodic benefit-risk evaluations. Collaborate with medical experts to identify and prioritize safety concerns.
