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