Drug Safety Specialist/Clinical Safety Coordinator

Responsibilities

• Determine the plan of action for incoming calls regarding safety inquiries
• Collect, process, and track incoming adverse and serious adverse events
• Write detailed safety narratives
• Report on various safety data sets
• Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes

Requirements

• Bachelor's degree in a healthcare-related field (e.g., Nursing, Pharmacy, Pharmacology)
• Proficient English communication skills
• Proficient knowledge of Microsoft Office
• Broad knowledge of medical terminology
• Strong organizational and communication skills

Preferred Qualifications

• Clinical experience or experience in Clinical Research
• Experience in case processing and Post-marketing Pharmacovigilance

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Flexible work environment
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing 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 a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, we employ more than 6,000 people across 40+ countries.