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.
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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 / RegVault
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- Regulatory Information Management (RIM)
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- Data Entry Requests (DER)
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- Registration Objects (RO)
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- Submission Objects (SO)
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- xEVMPD
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- IDMP
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- Regulatory Data Management
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nRoles & Responsibilities
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- Process Data Entry Requests (DERs) in Veeva RIM.
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- Create and maintain Registration Objects (ROs) and Submission Objects (SOs).
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- Perform regulatory data entry, validation, and reconciliation activities.
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- Manage submission records and health authority correspondence.
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- Support regulatory reporting, audits, and inspection readiness.
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- Maintain xEVMPD and IDMP data in compliance with regulatory requirements.t
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