Medpace Hiring for Study Start-Up Submissions Coordinator
Are you looking to advance your career in clinical research? Medpace, a global leader in clinical trial services, is hiring a Study Start-Up Submissions Coordinator for their Clinical Operations team in Navi Mumbai. This exciting opportunity allows you to contribute to innovative projects and shape the future of clinical development. Medpace Hiring for Study Start-Up Submissions Coordinator
About Medpace
Medpace is a top-tier, full-service clinical contract research organization (CRO) specializing in Phase I-IV clinical development. Headquartered in Cincinnati, Ohio, Medpace operates in over 40 countries with a workforce of more than 5,000 professionals. Medpace Hiring for Study Start-Up Submissions Coordinator
Therapeutic Expertise:
- Oncology
- Cardiology
- Central Nervous System Disorders
Their mission is to accelerate the development of safe and effective medical therapeutics through a scientific and disciplined approach.
Job Details
- Position: Study Start-Up Submissions Coordinator
- Location: Navi Mumbai
- Experience: Minimum 1 year in clinical research
- Salary: ₹4.8 – ₹5.3 LPA
- Qualifications: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, or a degree in Life Sciences
- Application Mode: Online
Key Responsibilities
As a Study Start-Up Submissions Coordinator, you will play a vital role in activating investigative sites for clinical trials. Below are the key responsibilities of this position:
Document Preparation and Submission
- Prepare, review, and submit required documents to regulatory agencies and ethics committees.
- Ensure accuracy and compliance with guidelines and regulations.
Coordination and Communication
- Act as the primary contact for submission-related activities during study initiation.
- Collaborate with global study teams to monitor study progress.
- Maintain communication with investigative sites throughout the activation process.
Risk Identification and Mitigation
- Identify potential risks in site activation processes.
- Implement mitigation strategies to ensure smooth operations.
Compliance and Expertise
- Provide guidance on ICH-GCP guidelines and evolving regulatory requirements.
- Advise sponsors on regulatory compliance for successful submissions.
Required Qualifications and Skills
Educational Background
- A Bachelor’s degree in science or a related field is mandatory.
Professional Experience
- A minimum of 1 year of experience in a CRO, pharmaceutical company, or investigative site.
- Hands-on expertise in preparing and submitting regulatory documentation.
Key Skills
- Strong organizational and communication abilities.
- Proficiency in Microsoft Office tools.
- In-depth knowledge of ICH-GCP guidelines and regulatory standards.
- Fluency in English, both written and verbal.
Why Choose Medpace?
Medpace offers a collaborative work environment designed to foster professional growth and innovation. Here’s why Medpace is an excellent career choice:
Work Environment
- Flexible work schedules to promote a healthy work-life balance.
- Encouragement of innovative thinking and teamwork.
Career Growth
- Structured paths for career development.
- Opportunities to work on groundbreaking clinical research projects.
Perks and Benefits
- Competitive salary and Paid Time Off (PTO) packages.
- Company-sponsored appreciation events.
- Health and wellness programs for employees.
Global Recognition
- Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
- Winner of multiple CRO Leadership Awards from Life Science Leader magazine.
How to Apply
Ready to take the next step in your clinical research career? Submit your application online for the Study Start-Up Submissions Coordinator position at Medpace in Navi Mumbai.
Don’t miss this opportunity to join a global leader in clinical research and make a meaningful impact in the field of medical therapeutics!
By joining Medpace, you’ll not only gain a rewarding role but also be a part of a company committed to shaping the future of healthcare. Apply today!
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