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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