JD FORMAT Copilot said: Job Title: Regulatory Information Management (RIM) Associate Experience: 1 Year Location: Open Qualification: B.Pharma, M.Pharma, Nursing, Life Sciences, Microbiology, Biochemistry, Zoology, Statistics, or related fields. Job Description We are looking for a Regulatory Information Management (RIM) Associate with hands-on experience in Veeva RIM/RegVault and regulatory data management activities. Mandatory Skills Veeva RIM / RegVault Regulatory Information Management (RIM) Data Entry Requests (DER) Registration Objects (RO) Submission Objects (SO) xEVMPD IDMP Regulatory Data Management Roles & Responsibilities Process Data Entry Requests (DERs) in Veeva RIM. Create and maintain Registration Objects (ROs) and Submission Objects (SOs). Perform regulatory data entry, validation, and reconciliation activities. Manage submission records and health authority correspondence. Support regulatory reporting, audits, and inspection readiness. Maintain xEVMPD and IDMP data in compliance with regulatory requirements.t

📌 RIMS Associate (Karnataka)
🏢 Tata Consultancy Services
📍 Karnataka