Drug Safety Specialist/ Clinical Safety Coordinator

Role & Responsibilities
• Handle and process adverse events and serious adverse events from all sources including clinical trials and post-marketing surveillance
• Determine appropriate plan of action for incoming safety-related calls
• Collect, process, document, and track safety case information accurately
• Write clear and compliant safety narratives
• Prepare and report safety data as per internal and regulatory requirements
• Collaborate with internal teams and investigative clinical research sites
• Ensure compliance with clinical safety and pharmacovigilance processes

Qualification
• Bachelor’s degree in a healthcare-related field
• Nursing, Pharmacy, Pharmacology, or equivalent qualification preferred

Experience
• Clinical experience or experience in clinical research preferred
• Exposure to case processing or post-marketing pharmacovigilance is an advantage

Skills
• Proficient English communication skills
• Strong knowledge of medical terminology
• Proficiency in Microsoft Office tools
• Excellent organisational and documentation skills
• Strong written and verbal communication abilities
• Ability to work in an office-based clinical safety environment

About the Company
• Medpace is a full-service global Contract Research Organization (CRO) Provides Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries.