Pharmacovigilance Associate: Safety & Regulatory Reporting

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

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