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