Drug Safety Specialist/ Clinical Safety Coordinator

Role & Responsibilities
• Determine the plan of action for incoming calls related to adverse events
• Collect, process, and track incoming adverse and serious adverse events
• Write safety narratives to document clinical events in the clinical trial process
• Report on various safety data related to clinical trials and post-marketing surveillance
• Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes

Qualifications
• Bachelor’s degree in Healthcare-related fields (Nursing, Pharmacy, Pharmacology, etc.)
• Clinical experience or Clinical Research, case processing, and Post-marketing Pharmacovigilance experience is preferred
• Proficiency in medical terminology and clinical safety procedures

Skills
• Strong organizational and communication skills
• Proficiency in English (written and spoken)
• Proficient knowledge of Microsoft® Office
• Broad knowledge of medical terminology
• Ability to work collaboratively across teams
• Strong attention to detail and ability to manage data accurately

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

About The Company
• Medpace is a full-service clinical contract research organization (CRO), offering Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.