Medical Monitor - Safety Analyst Clinical Trial/CRO
Listed on 2026-01-12
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Healthcare
Healthcare Management
Join to apply for the Medical Monitor - Safety Data Analyst I role at NSF.
The Medical Monitor/ Safety Data Analyst processes Adverse Event (AE) and Serious Adverse Event (SAE) cases promptly and with medical accuracy. The role also involves assisting the Head of Safety and Pharmacovigilance Department with Medical Coding and Medical Monitoring activities, overseeing the conduct of pre- and post-marketing studies regarding safety, and serving as a backup for other Medical Monitors.
Responsibilities include:
- Overseeing the conduct of safety studies.
- Performing medical reviews of study documents.
- Interacting with sponsors and clients.
- Developing pharmacovigilance and safety management plans.
- Leading coding procedures for medications and adverse events.
- Preparing safety reports for regulatory agencies.
- Maintaining safety databases and evaluating safety trends.
- Ensuring compliance with regulations and participating in audits and meetings.
Qualifications:
- Medical Degree (M.D./D.O.) required.
- Knowledge of global safety regulations.
- Experience with safety data processing systems preferred.
- Excellent communication skills.
- Experience with safety audits, EDC systems, MedDRA, and WHODrug is preferred.
About NSF:
With over 80 years of legacy, NSF leverages science and innovation to improve health and safety worldwide. We are committed to diversity and equal opportunity employment.
This job is active and accepting applications.
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