Dental Insurance, Vision Insurance, 401K, Medical Insurance
Full-Time | On-site
Job Description
We are seeking a dedicated Drug Safety Associate to support pharmacovigilance activities and ensure the safety of pharmaceutical products throughout their lifecycle. The successful candidate will review adverse event reports, monitor product safety data, maintain pharmacovigilance databases, and ensure compliance with FDA, EMA, and global regulatory requirements.
The Drug Safety Associate will collaborate with clinical research teams, regulatory affairs professionals, medical reviewers, and quality assurance personnel to evaluate safety information and contribute to risk management activities.
Responsibilities
- Process adverse event reports.
- Evaluate drug safety information.
- Ensure regulatory compliance.
- Prepare safety reports.
- Collaborate with clinical teams.
- Review medical documentation.
- Monitor global safety trends.
Education
- Bachelor's degree in Pharmacy, Life Sciences, Nursing, Medicine, or related field.
Required Skills
- Drug Safety
- FDA Regulations
- GCP
- MedDRA
- Medical Terminology
- Clinical Research
- Data Entry
- Attention to Detail
- Communication
Experience
- 1–3 years of pharmacovigilance or clinical safety experience.
Drug Safety Associate in iowa at Unknown Company
This position is listed as full time and onsite.