Regulatory Submissions Coordinator (Senior/ Experienced)
Regulatory Submissions Coordinator (Senior/ Experienced)
Medpace
Job description
Looking to advance your career in regulatory submissions and CRO operations? Explore this Regulatory Submissions Coordinator role at Medpace in Navi Mumbai.
Company Description
Medpace is a Contract Research Organization. The company offers development services from Phase I to Phase IV for pharmaceutical, biotechnology and medical device companies. With than 6,500 staff members spread across more than 40 nations Medpace speeds up the creation of safe and effective medical treatments worldwide. Medpace carries in‑country regulatory and therapeutic expertise, in major clinical research areas.
Job Summary
This senior or experienced level role is based in Navi Mumbai, within Medpace's Clinical Operations team. As a Regulatory Submissions Coordinator, you will manage site activation, ethics committee filings, and regulatory dossier submissions across Phase I to IV trials. You will work closely with CDSCO and DCGI processes through the SUGAM portal. The role also involves close coordination with global study teams throughout each trial.
Key Responsibilities
Manage site activation activities for clinical trials across different phases.
Prepare and submit regulatory documentation to relevant health authorities.
Handle ethics committee filings as part of the site activation process.
Review essential documents required to activate study sites.
Coordinate CDSCO and DCGI submissions through the SUGAM online portal.
Collaborate with global study teams to keep submissions on track.
Provide knowledge and help to internal teams whenever they need it.
Keep track and ensure timely submission of required documents.
Maintain records of every regulatory form and all related messages.
Educational Qualification
Bachelor's or Master's degree in Science, Pharmacy, or Life Sciences.
Skills Required
4 or more years of experience in the relevant field.
Hands on experience in clinical regulatory submissions, EC filings, and site activation within a CRO or pharma company.
Deep understanding of CDSCO, DCGI, and SUGAM portal procedures.
Strong knowledge of India's clinical trial regulatory framework.
Good communication and coordination skills to work with global teams.
Strong attention to detail and document accuracy.
Ability to manage multiple submissions and deadlines at once.
Salary Structure
The salary for a Regulatory Submissions Coordinator at Medpace Clinical Research is typically ranges from ₹10 Lakhs to ₹16 Lakhs per year.
Career Development
This role offers hands on exposure to India's regulatory submission process within a respected global CRO. Medpace also supports long term growth through structured processes, mentorship, and opportunities to build deeper expertise in clinical regulatory affairs.
How to Apply
Visit our job portal and search for the Regulatory Submissions Coordinator role in Medpace.
Click on the job posting to read all the details about the job.
Fill in your details. Upload your updated resume.
Send your application.
Education
Bachelor's Degree
Key Skills
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