RIMS Associate

Job Description

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

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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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Roles & 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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