๐Ÿš€ Career Opportunity: Sr. Product Integrator (ISG) โ€“ Chennai, India

Are you a seasoned professional with expertise in clinical systems integration? Do you have hands-on experience with RAVE and Veeva Vault for eTMF? If you’re ready to take on a strategic role in a hybrid work environment, we have an exciting opportunity for you!

๐Ÿง  Job Title: Sr. Product Integrator (ISG)

Location: Chennai, India

Work Model: Hybrid

Employment Type: Full-time

Job Category: Technology & Engineering

Job Number: 00064705212

Travel Required: No

Date Published: September 30, 2025

๐Ÿ“‹ Job Summary

The Sr. Product Integrator (ISG) will play a pivotal role in integrating and managing product solutions within our organisation. This role focuses on the deployment and optimisation of RAVE and Veeva Vault for eTMF, ensuring seamless operations, regulatory compliance, and enhanced document management processes.

This position is ideal for professionals who thrive in a hybrid work model and are passionate about improving clinical systems through strategic integration and technical leadership.

๐Ÿ”ง Key Responsibilities

As a Sr. Product Integrator, your responsibilities will include:

Leading the integration of RAVE and Veeva Vault for eTMF to streamline ,clinical documentation workflows.

Overseeing the configuration and deployment of eTMF systems to meet industry and regulatory standards.

Providing technical expertise in managing and troubleshooting RAVE and Veeva Vault applications.

Collaborating with cross-functional teams to align product integration with business goals.

ย Developing strategies to improve the efficiency and reliability of eTMF systems.

 Monitoring system performance and recommending enhancements.

 Ensuring data integrity, security, and compliance across all eTMF platforms.

ย Conducting regular audits to maintain regulatory compliance.

 Facilitating training sessions for internal teams on system usage and best practices.

 Supporting R&D initiatives with technical insights and integration support.

 Coordinating with stakeholders to gather requirements and deliver tailored solutions.

 Documenting integration processes and maintaining comprehensive records.

Contributing to continuous improvement initiatives in product integration methodologies.

 ๐ŸŽ“ Qualifications

To be successful in this role, candidates must meet the following criteria:

 Minimum 5 years of experience in RAVE and Veeva Vault for eTMF.

 Proven expertise in managing electronic trial master files (eTMF) within a regulated environment.

 Strong understanding of clinical research and development processes.

 Experience working in hybrid work models, balancing remote and on-site collaboration.

 Proficiency in troubleshooting and resolving technical issues related to    eTMF systems.

 Excellent communication and documentation skills.

๐ŸŒ Why Join Us?

This role offers a unique opportunity to work at the intersection of technology and clinical research. Youโ€™ll be part of a forward-thinking team that values innovation, compliance, and collaboration. Our hybrid work model ensures flexibility while maintaining strong team engagement and productivity.

๐Ÿ“ฉ Ready to Apply?

If you meet the qualifications and are excited about this opportunity, we encourage you to apply today. This is your chance to contribute to meaningful clinical research and technology integration.

๐Ÿ“Œ Apply Now or share this opportunity with someone who fits the role!: https://careers.cognizant.com/global-en/jobs/00064705212/veeva-vault-etmf-ctms-isg/?source=JB-11500

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