Drug Safety Associate

myBridge Corporation; Princeton (NJ); On-site; USD 90,000 - 110,000; Full time

Job summary

myBridge Corporation in Princeton, New Jersey, USA is seeking a Drug Safety Associate to monitor the safety of pharmaceutical products. You will collect adverse event reports, evaluate cases, and prepare submissions to regulatory authorities.

The role collaborates with clinical research, regulatory affairs, and healthcare professionals to ensure compliance with international pharmacovigilance guidelines. Strong analytical skills and attention to detail are essential; career path includes senior

Qualifications

• Bachelor's or Master's degree in Pharmacy, Life Sciences, Nursing, Biotechnology, Medicine, or related healthcare discipline.
• Knowledge of pharmacovigilance regulations is preferred.

Responsibilities

• Monitor safety of medicines by collecting, evaluating, and reporting adverse drug reactions.
• Prepare safety reports and submissions to regulatory authorities.
• Collaborate with clinical research, regulatory affairs and healthcare professionals to ensure compliant pharmacovigilance documentation.

Skills

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.

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.