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
- 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
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