About this opportunity
myBridge Corporation lists this Drug Safety Associate opportunity in princeton, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
princeton, NJ, 08543, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.