Biology Jobs at Medpace
Medpace is seeking a Drug Safety Associate (Clinical Safety Coordinator) to join its Clinical Safety team in Cincinnati, Ohio. This is a full-time, office-based role. The Biology Jobs at Medpace focus on processing and managing adverse event data from clinical trials and post-marketing surveillance. It is an excellent opportunity for life sciences graduates looking to build a long-term career in pharmacovigilance and clinical safety within a global CRO environment.
Job Details:
- Job Title: Drug Safety Associate (Clinical Safety Coordinator)
- Job Type: Full-Time
- Location: Cincinnati, Ohio, USA
- Department: Clinical Safety
- Job ID: 12347
- Industry: Contract Research Organization (CRO)
About the Company:
Medpace is a full-service global Contract Research Organization (CRO) providing Phase I–IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries. The company supports therapeutic areas including oncology, cardiology, metabolic diseases, endocrinology, CNS, antiviral, and anti-infective research, with a strong reputation for scientific rigor and operational excellence.
Educational Requirements for the Drug Safety Associate Role:
-
Bachelor’s degree in Life or Health Sciences, including but not limited to Biology, Microbiology, or related scientific disciplines
Key Responsibilities:
- In this Drug Safety Associate Role, you have to collect, process, and track Serious Adverse Event (SAE) reports.
- Perform safety database data entry with high accuracy
- Generate safety narratives and follow-up queries
- Conduct quality control (QC) checks of safety cases as a Drug Safety Associate.
- Collaborate with internal teams and investigative clinical research sites
- Ensure compliance with clinical safety and pharmacovigilance processes
- Support ongoing safety operations for clinical trials and post-marketing activities
Skills Required:
- Broad understanding of medical terminology
- Strong organizational and documentation skills
- Proficiency in Microsoft Office (Word, Excel, Outlook) are required for the Drug Safety Associate Role.
- Close attention to detail and data accuracy
- Strong written and verbal communication skills
- Ability to work effectively in a regulated clinical research environment
Benefits of the Biology Jobs at Medpace:
- Structured career paths with long-term professional growth opportunities
- Competitive compensation and comprehensive benefits package
- Flexible work environment
- Competitive PTO starting at 20+ days
- Modern, eco-friendly campus with on-site fitness center
- Employee health and wellness initiatives
- Company-sponsored appreciation events
- Community involvement with local nonprofit organizations
- Discounts on sports events, fitness centers, and local attractions
- Discounted tuition for University of Cincinnati online programs
