Assoc Clin DB Validation Mgr

iqvia· RPL IQVIA RDS (India) Private Limited
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About this role

Job Overview
Manage end-to-end delivery of testing services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive testing expertise to testing team to provide high quality database that meet customer requirements. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.

Essential Functions
• Attend Kick Off Meeting and regular project meetings until Study Go Live.
• Take complete responsibility for creation of Edit Checks Test Plan document and writing test cases.
• Release the Edit Checks Test Plan to the testing team to conduct testing activities.
• Review Project Plan and escalate issues (if any) to all stakeholders.
• Comprehend study protocol and share the basic requirement of protocol with validation project team.
• Perform eCRF and Time & Events QC as per QC checklist.
• Test email alerts
• Review ASB and Edit Specification document, provide input and escalate issues if any.
• Document in version history if any changes made to Edit Specifications within Test Plan during validation process.
• Request final and authorized version of documents to validate system configuration (AUL, Rights and Roles, Home page, System Settings).
• Provide project status updates on validation activities to Data Team Lead/Lead Programmers.
• Review Testing Comments Log after each cycle of testing and provide Testing Comments Log to Programmer.
• Document all testing documentation in eDMSF in a timely manner.
• Co-ordinate with internal Customers on a regular basis and establish strong Communications with them.
• Work with functional manager(s) to ensure appropriate resources are assigned to meet project deliverables.
• Implement proactive quality management plans across multiple projects/programmes.  Track service performance and provide leadership to identify root cause of issues and implement remedial actions.
• Continuously look for opportunities to improve the process; work with team to develop and implement plan to re-organize and drive change across multiple projects/programme (with minimal support)
• Ensure timely follow-up and resolution of compliance issues.
• Serve as Subject Matter Expert (SME) for validation group.
• Train and mentor Testing Team Members.
• Provide end to end Project Management for testing activities in the team, e.g. proactive and accurate resource planning, planning for deliverables, identifying
• risks (if any) and escalate such risks to the Manager.
• Conduct Quality Reviews as applicable.
• Review the QIP for appropriate budget allocation and communicate if any out of scope activities are noted.
• Review individual project financial performance and communicate issues to the appropriate stakeholders.  Ensure adherence to study budgets.
• Supervise implementation of new technology.
• Serve as primary point of contact for Internal Customers on testing deliverables.
• Provide justification for and perform direct negotiations with Internal Customers, e.g., timelines, financial, process, resources.
• Develop and maintain strong Customer relationships.
• All responsibilities are essential job functions unless noted as nonessential (N).

Qualifications
• Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology  Req
• 4- 6 years of relevant clinical DB Testing experience in CDMS Platforms and total exp being 6+ yrs Req

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Frequently Asked Questions

Is the salary disclosed for the Assoc Clin DB Validation Mgr position at iqvia?
The salary for this Assoc Clin DB Validation Mgr role at iqvia is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Assoc Clin DB Validation Mgr position at iqvia located?
This Assoc Clin DB Validation Mgr role at iqvia is based in Bangalore, India, Kolkata, West Bengal, India. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Assoc Clin DB Validation Mgr role at iqvia full-time or part-time?
This is listed as a Full time position. It is posted as a Assoc Clin DB Validation Mgr role in the RPL IQVIA RDS (India) Private Limited department at iqvia.
Which team or department does the Assoc Clin DB Validation Mgr at iqvia belong to?
This Assoc Clin DB Validation Mgr position is part of the RPL IQVIA RDS (India) Private Limited department at iqvia. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Assoc Clin DB Validation Mgr position at iqvia?
Click the "Apply Now" button on this page. You will be redirected to iqvia's official application portal hosted on workday where you can submit your application directly.
When was the Assoc Clin DB Validation Mgr job at iqvia posted?
This Assoc Clin DB Validation Mgr position at iqvia was posted on Sep 17, 2026. Apply as soon as possible — early applications are often reviewed first.
Assoc Clin DB Validation Mgr
iqvia
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