Job Description
JD FORMAT
nCopilot said:
nJob Title: Regulatory Information Management (RIM) Associate
nExperience: 1+ Year
nLocation: Open
nQualification: B.Pharma, M.Pharma, Nursing, Life Sciences, Microbiology, Biochemistry, Zoology, Statistics, or related fields.
nJob Description
nWe are looking for a Regulatory Information Management (RIM) Associate with hands-on experience in Veeva RIM/RegVault and regulatory data management activities.
nMandatory Skills
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- Veeva RIM / RegVaultn
- Regulatory Information Management (RIM)n
- Data Entry Requests (DER)n
- Registration Objects (RO)n
- Submission Objects (SO)n
- xEVMPDn
- IDMPn
- Regulatory Data Managementn
nRoles & Responsibilities
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- Process Data Entry Requests (DERs) in Veeva RIM.n
- Create and maintain Registration Objects (ROs) and Submission Objects (SOs).n
- Perform regulatory data entry, validation, and reconciliation activities.n
- Manage submission records and health authority correspondence.n
- Support regulatory reporting, audits, and inspection readiness.n
- Maintain xEVMPD and IDMP data in compliance with regulatory requirements.tn