Clinical Safety Coordinator

at  Medpace Inc

Job Summary:
We are currently seeking a full-time, office-based Clinical Safety Nurse to join our Clinical Safety department. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.
If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

Responsibilities :

• Collect, process, and track serious adverse event (SAE) reports
• Generate safety narratives and queries
• Safety database data entry
• Perform quality control of safety cases
• Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.

Qualifications :

• Bachelor’s degree in life/health science including, but not limited to, Microbiology, Biology, Nursing, Pharmaceutical Science, Chemistry, or related field;
• Clinical experience or Clinical Research/Post marketing Pharmacovigilance experience is preferred;
• Proficient knowledge of Microsoft® Office;
• Broad knowledge of medical terminology; and
• Strong organizational and communication skills.

Medpace Overview :
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

• Collect, process, and track serious adverse event (SAE) reports
• Generate safety narratives and queries
• Safety database data entry
• Perform quality control of safety cases
• Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes