Medpace
Clinical Safety Coordinator (Life Sciences Degrees)
Medpace, Cincinnati, Ohio, United States, 45208
Overview
Clinical Safety Coordinator (Life Sciences Degrees). We are seeking a full-time, office-based Clinical Safety Coordinator 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. 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, Pharmaceutical Science, Chemistry, or related field Proficient knowledge of Microsoft Office Broad knowledge of medical terminology Strong organizational and communication skills About Medpace
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. What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Clinical Safety Coordinator (Life Sciences Degrees). We are seeking a full-time, office-based Clinical Safety Coordinator 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. 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, Pharmaceutical Science, Chemistry, or related field Proficient knowledge of Microsoft Office Broad knowledge of medical terminology Strong organizational and communication skills About Medpace
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. What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
#J-18808-Ljbffr