Medpace, a leading global Clinical Research Organization (CRO), is hiring a full-time eClinical Coordinator in Navi Mumbai, India. This role is ideal for detail-oriented professionals passionate about clinical data management and ensuring the accuracy of patient-reported outcomes in global clinical studies.
If you’re looking to build a career in clinical research operations and grow within a company recognized globally for excellence, this is your chance to join a world-class team.
🧩 Key Responsibilities
As an eClinical Coordinator, you will play a pivotal role in supporting data accuracy and compliance for clinical trials. Your daily activities will include:
- Assisting Project Managers in system design and eClinical setup.
- Creating study-specific documentation and maintaining quality records.
- Tracking and reporting key study metrics and progress.
- Collaborating with clients to gather requirements and resolve queries.
- Performing other assigned data management and eClinical tasks.
🎓 Qualifications & Requirements
To excel in this role, candidates should meet the following criteria:
- Bachelor’s degree in a health-related field (e.g., Pharmacy, Life Sciences, Biotechnology).
- Strong attention to detail and proficiency in Microsoft Excel and Word.
- Working knowledge of medical terminology.
- 1–2 years of experience in a pharmaceutical or CRO setting preferred.
- No travel required.
💼 Why Join Medpace?
At Medpace, employees are the foundation of success. The organization offers:
- A flexible work environment with hybrid options.
- Competitive salary and benefits package.
- Generous paid time off (PTO) and wellness initiatives.
- Structured career growth and professional development programs.
- Regular employee appreciation events and recognition.
Medpace has been recognized by Forbes (2021–2024) as one of America’s Most Successful Midsize Companies and consistently earns CRO Leadership Awards for quality, reliability, and expertise.
📝 How to Apply
