Washington, District of Columbia, United States Full-Time | On-site Drug Safety Associate Location: Princeton, New Jersey, USA Job Description A Drug Safety Associate is responsible for monitoring the safety of pharmaceutical products by collecting, evaluating, and reporting adverse drug reactions. They help ensure compliance with global pharmacovigilance regulations and contribute to patient safety. Skills Required Drug Safety Reporting Medical Terminology Clinical Research Regulatory Compliance Data Analysis Case Processing Attention to Detail Communication Skills Microsoft Office Medical Writing Education Bachelor's or Master's degree in Pharmacy, Life Sciences, Nursing, Biotechnology, Medicine, or related healthcare discipline. Description Drug Safety Associates play an important role in monitoring the safety profile of medicines throughout their lifecycle. They collect adverse event reports from healthcare professionals and patients, assess case validity, perform medical coding, and prepare reports for submission to regulatory authorities. The role requires collaboration with clinical research teams, regulatory affairs specialists, and healthcare professionals to ensure accurate safety documentation and compliance with international pharmacovigilance guidelines. Strong analytical skills, knowledge of medical terminology, and attention to detail are essential. Career growth includes Senior Drug Safety Associate, Pharmacovigilance Scientist, Drug Safety Manager, and Regulatory Affairs Specialist. #J-18808-Ljbffr
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