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Pharmacovigilance Physician Jobs

10 Job Offers

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Clinical Study Physician - Oncology
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United States , Remote
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Parexel
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Study Physician - Oncology - FSP
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United States
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Parexel
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Clinical Study Physician - Oncology - FSP
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United States , Remote
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Parexel
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Study Physician - Oncology trials
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Germany
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Parexel
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Key Account Manager aHUS
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Germany , München
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Proclinical
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Patient Access Navigator
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Canada
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85035.00 - 103438.00 CAD / Year
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Amgen
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Pharmacovigilance Physician
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United Kingdom , Guildford
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PrimeVigilance
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Medical Information Associate
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United Kingdom , Guildford
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PrimeVigilance
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Senior Physician, Patient Safety
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United States; Canada , Remote; Alberta
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Parexel
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Associate Director, Pharmacovigilance Scientist
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United States , Waltham
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160000.00 - 200000.00 USD / Year
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Kailera Therapeutics
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Discover rewarding and critical pharmacovigilance physician jobs, a specialized medical career at the heart of patient safety and public health. Pharmacovigilance physicians are licensed medical doctors who apply their clinical expertise to the scientific discipline of monitoring and evaluating the safety of pharmaceutical products, both before and after they reach the market. These professionals serve as the crucial medical voice within pharmacovigilance (PV) departments, ensuring that the benefit-risk profile of medicines is continuously and rigorously assessed. Their work is fundamental to protecting patients and informing regulatory decisions worldwide. The core responsibility of a pharmacovigilance physician is the medical assessment of individual safety reports. This involves reviewing cases of adverse events from clinical trials and post-marketing surveillance to determine causality, seriousness, expectedness, and clinical significance. They provide the medical analysis and company commentary for these reports, which are submitted to global health authorities. Beyond case processing, PV physicians play a strategic role in risk management. They analyze aggregate safety data, author or review periodic safety reports (like PSURs and DSURs), and contribute to the development of Risk Management Plans (RMPs). They are also key in evaluating potential safety signals, recommending actions, and providing medical input for safety queries from regulators or internal stakeholders. Furthermore, they often review medical literature for relevant safety information and may contribute to the medical content of protocols, informed consent forms, and safety sections of regulatory documents. Typical requirements and skills for pharmacovigilance physician jobs are stringent, reflecting the role's importance. An active medical degree (MD or equivalent) and license to practice are universally mandatory. While prior PV experience is highly valued, many organizations offer entry-level positions for physicians seeking to transition from clinical practice. Essential skills include a meticulous, analytical mindset with strong attention to detail, as decisions have significant regulatory and patient implications. Excellent written and verbal communication skills are paramount for articulating complex medical safety analyses. Physicians must be proficient in interpreting clinical data, understanding regulatory guidelines (ICH, GVP), and often have a working knowledge of relevant medical coding dictionaries like MedDRA. The ability to work collaboratively within cross-functional teams, manage multiple priorities, and maintain a proactive, patient-centric approach is critical. For those with the right medical foundation, pharmacovigilance physician jobs offer a unique, intellectually stimulating, and impactful career path outside traditional clinical settings, directly contributing to the safe use of medicines on a global scale.

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