Padmi

Veeva Vault RIM - Regulatory Business Analyst

Remote · (Piscataway, NJ, 08854)Posted 2 months ago
Computer Systems AnalysisUnspecified
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Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Veeva Vault RIM Consultant position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: Regulatory Business Analyst - Veeva Vault RIM

Location: Remote

Duration: 6-Month Contract

Experience: 5–6 Years

Job Overview

We are seeking a Regulatory Business Analyst with strong expertise in Veeva Vault RIM to support regulatory operations, data remediation, system enhancements, and business process optimization. The ideal candidate will have experience with regulatory information management, validation activities, and digital transformation initiatives within a regulated life sciences environment.

Key Responsibilities

Support configuration, maintenance, and business processes within Veeva Vault RIM.

Perform regulatory data remediation and ensure data quality and integrity.

Support IDMP, eCTD, and regulatory submission processes.

Manage integrations between Veeva Vault Quality and Veeva Vault RIM.

Develop and monitor RIM reports, dashboards, and KPIs.

Coordinate UAT, review test scripts, and support system validation activities.

Create and maintain SOPs, training materials, and user documentation.

Collaborate with cross-functional teams on AI/GenAI, automation, and digital transformation initiatives.

Support continuous process improvements within regulatory systems.

Required Qualifications

Bachelor's degree in Life Sciences, Information Systems, or a related field.

5+ years of experience as a Business Analyst supporting Regulatory Affairs systems.

Strong hands-on experience with Veeva Vault RIM (configuration, data model, and business process support).

Experience with data remediation, IDMP, eCTD, and SDLC.

Knowledge of Veeva Vault Quality–RIM integrations.

Experience supporting validation activities, including UAT and test script reviews.

Strong documentation skills with experience creating SOPs and training materials.

Exposure to AI/GenAI, automation, or digital transformation initiatives.

Familiarity with eCTD publishing solutions; eCTD 4.0 experience is a plus.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com

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