Medpace is seeking a Clinical Safety Coordinator to join our Clinical Safety department full-time in India. The role involves handling and processing adverse events from multiple sources, including clinical trials and post-marketing surveillance. This is an exciting opportunity to grow your career and make a significant impact in clinical safety.
Key Responsibilities:
- Manage incoming calls and determine appropriate action.
- Collect, process, and track adverse and serious adverse events.
- Write comprehensive safety narratives.
- Generate reports on safety data.
- Collaborate with internal teams and clinical research sites to ensure adherence to safety processes.
Qualifications:
- Bachelor’s degree in healthcare-related fields such as Nursing, Pharmacy, or Pharmacology.
- Preferred experience in Clinical Research, case processing, and Post-Marketing Pharmacovigilance.
- Proficient in English and Microsoft® Office.
- Strong knowledge of medical terminology.
- Excellent organizational and communication skills.
Why Join Medpace?
Medpace is a leading clinical contract research organization (CRO) with over 30 years of experience in developing medical therapeutics. With headquarters in Cincinnati, Ohio, and over 5,000 employees across 40+ countries, Medpace is dedicated to accelerating global development in critical therapeutic areas.
Perks & Benefits:
- Hybrid work-from-home options (dependent on position and level).
- Competitive PTO packages.
- Employee appreciation events.
- Health and wellness initiatives.
- Flexible work schedule.
- Competitive salary and benefits package.
- Opportunities for professional growth.
Awards:
- Featured by Forbes as one of America’s Most Successful Midsize Companies (2021-2024).
- CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility.
