Associate - Regulatory Affairs (RegPoint)

Roles & Responsibilities:
• Perform regulatory data clean-up activities in the Regulatory Information Management System (RIMS).
• Review and validate regulatory data entered by business users to ensure accuracy and completeness.
• Process submission intake requests and handle ticket-based user requests.
• Communicate with internal stakeholders to resolve regulatory data-related queries.
• Ensure daily task completion in line with defined RIMS processes and timelines.
• Collect regulatory information from multiple manual and electronic sources.
• Enter, update, and maintain regulatory data in RIMS for compliance and analysis.
• Perform peer quality checks against source regulatory documents.
• Support documentation management and audit-readiness activities.

Qualification:
• B.Pharm or M.Pharm (mandatory)

Experience:
• Freshers are eligible
• 3 to 6 months of experience in RIMS or regulatory data management will be an advantage

Skills:
• Working knowledge of MS Office (Word, Excel, Outlook)
• Exposure to RIMS and document management systems (preferred)
• Excellent written and verbal communication skills in English
• Strong attention to detail with a compliance-focused mindset
• Ability to manage routine regulatory tasks efficiently

About the Organization:
ClinChoice is a globally recognized clinical research and regulatory services organization founded in 1995, providing end-to-end support across regulatory affairs, clinical operations, biometrics, pharmacovigilance, and medical affairs, with a strong global footprint and advanced regulatory technology capabilities supporting compliant and efficient product development worldwide.