Roles and Responsibilities :
Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials;
Prepare, review, and submit to Regulatory Agencies;
Communicate with global study teams and personnel on study progress;
Ability to effectively identify risks to site activations and mitigate as necessary;
Provide expertise and guidance to global study teams in ethics and regulatory submissions;
Review and finalize essential documents required for site activation;
Act as a main contact for Ethical and Regulatory submission-related activities;
Direct contact with investigative sites during the study start up and activation process;
Ensure submissions comply with applicable regulations and guidance documents;
Advise sponsors on changing regulations and compliance requirements; and




Track submissions and ensure timely filing of documents.

Job Requirements :
Bachelor’s degree in science field and more than 4 years of regulatory submissions experience in clinical research, preferably with a CRO.
Hands-on experience preparing, reviewing, and submitting regulatory documentation to ECs and RA (minimum CDSCO and DCGI); including formulating responses to queries.
Open to travel to Delhi on ad-hoc basis will be a plus point.
Solid oral and written communication skills.
Position comesurate with experience. Robust Local experience mandatory for Regulatory Submissions Coordinator level, Local and Regional APAC experience mandatory for a Regulatory Submissions Manager level

📌 Regulatory Submissions Coordinator Mumbai
🏢 Medpace Clinical Research India
📍 Mumbai