*CBCC Global Research is hiring* *Position:* Regulatory Associate *Location:* Ahmedabad (Office-based) *Qualification:* B.Sc./M.Sc. or any relevant graduate degree *Experience:* 1–3 years – In CRO *CTC/Budget:* Best in Industry *Working Days* – 05 Days *Key Responsibilities:* Manage end-to-end regulatory submissions to CDSCO for clinical trials in India. Assess feasibility of clinical investigations per Indian regulations. Prepare and compile regulatory dossiers in consultation with the project manager. Conduct document gap analysis as per regulatory checklists. Ensure complete and timely online submissions via SUGAM and NSWS portals. Coordinate with regulatory consultants/agencies and sponsors. Handle post-approval activities and CTRI registration before patient enrolment. Maintain compliance with GCP, NDCTR 2019, SOPs, and quality standards. Track and report regulatory timelines, maintain trackers. Interested candidate can apply at [email protected]