RIMS Associate

Tata Consultancy Services; Bengaluru; On-site; INR 400,000 - 650,000; Full time

Job summary

Tata Consultancy Services is seeking a Regulatory Information Management (RIM) Associate to support regulatory data workflow. The role requires hands-on experience with Veeva RIM/RegVault and related DER/RO/SO operations.

You will perform data entry, validation, reconciliation, manage submission records and health authority correspondence, and assist with regulatory reporting, audits, and inspection readiness, ensuring xEVMPD/IDMP data alignment.

Qualifications

• Hands-on experience with Regulatory Information Management (RIM).
• Experience with Veeva RIM/RegVault and regulatory data management activities.
• Knowledge of DER/RO/SO processes within RIM.

Responsibilities

• Perform regulatory data entry, validation, and reconciliation activities.
• Create and maintain Registration Objects (ROs) and Submission Objects (SOs).
• Manage submission records and health authority correspondence.
• Support regulatory reporting, audits, and inspection readiness.
• Maintain xEVMPD and IDMP data in compliance with regulatory requirements.

Skills

Regulatory Information Management (RIM

Data Entry Requests (DER)

Regulatory Data Management

Process Data Entry Requests (DERs) inV

Education

B.Pharma, M.Pharma, Nursing, Life Sciences, Microbiology, Biochemistry, Zoology, Statistics, or related fields.

Tools

Veeva RIM

RegVault

Job description

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

• Regulatory Information Management (RIM)
• Data Entry Requests (DER)
• Registration Objects (RO)
• Submission Objects (SO)
• xEVMPD
• IDMP
• Regulatory Data Management
• 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