
1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
🕒 June 29
🏄 California, Pennsylvania – Remote
💵 $212k - $318k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏭 Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
• implementing the global safety strategy and monitoring the overall safety profile for products • generating all major pre- and post-marketing safety deliverables including signal and risk management activities • providing Medical Safety/PV inputs to assigned products and liaising with multiple departments • participating in the preparation and review of safety-related clinical and regulatory documents • conducting signal detection activities and ensuring communication of safety assessments to stakeholders • contributing to preparation of Risk Management Plans (RMPs) for assigned products
• MD required (or equivalent) • medical licensure in at least one state preferred • minimum 3 years of Drug Safety/Pharmacovigilance (PV) experience or 3 or more years clinical development experience • understanding of global PV regulatory environment with working knowledge of international regulations, GVP • working knowledge of safety databases (ARISg, ARGUS, or other safety database applications) • MedDRA trained and working knowledge of MedDRA and WHO Drug coding dictionaries • high level of initiative and independence • excellent written and oral communication skills • computer literacy with proficiency in external Regulatory Databases, Microsoft Excel, PowerPoint and Word
• medical, dental and vision insurance • 401k retirement savings plan • flexible paid vacation • discretionary annual cash bonus or incentive compensation • discretionary equity grants
Apply Now🕒 June 29
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