Are you passionate about advancing medical research and improving patient lives? Join a global leader in clinical research where your expertise will help bring life-changing therapies to patients worldwide!
Company: Medpace
Location: Navi Mumbai, India
Position: Study Start-up Submissions Coordinator
Department: Clinical Operations
About Medpace: 
- Global CRO with 5,000+ professionals across 40+ countries
- 30+ years of excellence in clinical research
- Forbes-recognized as America’s Most Successful Midsize Company (2021-2024)
- Expertise across all major therapeutic areas
Key Responsibilities: 
Manage site activation for clinical trials
Prepare and submit regulatory documentation
Collaborate with global study teams
Review essential documents for site activation
Provide regulatory expertise and guidance
Track and ensure timely document submissions
What They’re Looking For: 
Bachelor’s degree in science or equivalent experience- 1+ year experience in CRO, pharma, or research site
Knowledge of ICH-GCP and regulatory guidelines
Proficiency in Microsoft Office
Excellent communication skills
Strong command of English
Why Medpace? 
Hybrid work options available- Structured career growth paths
Competitive PTO and benefits
Employee appreciation events
Wellness initiatives
Flexible work schedule
Ready to accelerate global medical therapeutics development? Apply Here
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