Life Science Jobs In USA- Explore Medpace Careers & Apply Now For Drug Safety Associate Jobs
Life Science Jobs In USA- Are you passionate about patient safety and interested in building a career in pharmacovigilance and clinical research? Explore Medpace careers & join a global leader in clinical development, as a Drug Safety Associate (Clinical Safety Coordinator)- Drug safety associate jobs at our Cincinnati, Ohio headquarters. This full-time, office-based role offers a unique opportunity to apply your life sciences background to ensure the safety and effectiveness of new medical treatments worldwide. At Medpace, you’ll be part of a collaborative team dedicated to accelerating the development of life-changing therapies where your work directly impacts global health.
Life Science Jobs In USA- Details:
- Position: Drug Safety Associate
- Job ID: 11670
- Location: Cincinnati, Ohio, USA
About The Company:
Medpace is an award-winning, full-service Clinical Research Organization (CRO) providing comprehensive Phase I–IV development services to the pharmaceutical, biotechnology, and medical device industries. With operations in 40+ countries and a team of over 5,000 professionals, we specialize in therapeutic areas such as oncology, cardiology, metabolic disease, infectious diseases, endocrinology, and neurology. Our mission is clear — to accelerate the global development of safe and effective medical therapeutics through scientific precision, ethical research, and world-class operational excellence. Headquartered in Cincinnati, Ohio, Medpace continues to be recognized globally as a Top Workplace (2024) and a Forbes Most Successful Midsize Company (2021–2024).
Life Science Jobs In USA- Role:
As a Drug Safety Associate (Clinical Safety Coordinator), you will play a vital role in monitoring, collecting, and evaluating adverse event (AE) data from clinical trials and post-marketing sources. Your work will help safeguard patient welfare while ensuring regulatory compliance throughout the drug development process. This position is ideal for graduates in life sciences, pharmacy, biotechnology, or related fields who want to develop a long-term career in pharmacovigilance or clinical research.
Key Responsibilities
As part of Medpace’s Clinical Safety team, you will:
- Collect, process, and track serious adverse event (SAE) reports from multiple sources.
- Generate and review safety narratives and data queries to ensure case completeness.
- Perform data entry and quality control within global safety databases.
- Collaborate with internal departments, study teams, and clinical research sites to ensure safety process compliance.
- Assist in safety data analysis and contribute to global pharmacovigilance reporting efforts.
Drug Safety Associate Jobs- Qualifications
To be successful in this role, you should have:
- A Bachelor’s degree in Life Sciences or a related discipline (e.g., Biology, Microbiology, Pharmaceutical Sciences, Chemistry, Biochemistry).
- Strong understanding of medical terminology and clinical data.
- Proficiency in Microsoft Office and database management tools.
- Excellent organizational, analytical, and communication skills.
- Strong attention to detail and the ability to work in a fast-paced environment.
Explore Medpace Careers & Join Now
At Medpace, your career will thrive at the intersection of science, innovation, and purpose. We provide a structured, supportive environment that encourages professional growth and continuous learning.
