Headline

Manager, CDM | IQVIA | 15+ Years Driving Data Integrity in Clinical Research | AI practitioner in Large-Scale Data Systems & Process Optimization

About

With over 15 years of experience in clinical data management, I currently work as a Manager at IQVIA, where I oversee a team to ensure the delivery of high-quality data management projects. Major focus on enhancing skills on tools such as JIRA, Spotfire, copilot, any AI tool that is compliant to pharma industry. My expertise includes clinical data management and data analysis, utilizing tools such as Medidata to streamline operations and maintain data accuracy. At IQVIA, I focus on providing strategic oversight, effective resource allocation, and technical guidance to my team while upholding strict compliance with protocols and timelines. I remain committed to fostering continuous professional growth and leveraging my skills to enhance operational efficiency and ensure audit-ready outcomes.

Location

Bengaluru

AI stack

claude

gemini

grok

notion

openai

Bolt.new

Work experience

Manager at IQVIA, Apr 2026 - Present · 7 mos, India

Associate Manager at IQVIA, Mar 2024 - Apr 2026 · 2 yrs 2 mos, On-site

Data Team Lead at IQVIA, Feb 2021 - Feb 2024 · 3 yrs 1 mo, Bangalore Urban, Karnataka, India

Assistant Manager at Tata Consultancy Services, Jun 2018 - Feb 2021 · 2 yrs 9 mos, Thane, Maharashtra, India

Team leader at Cognizant, Apr 2017 - May 2018 · 1 yr 2 mos, Mumbai Area, India

CDA II (Clinical Data Analyst II) at Parexel International, Jun 2015 - Mar 2017 · 1 yr 10 mos, Greater Hyderabad Area,  Utilizing study documentation including protocol, CRFs, Cleaning guidelines etc.  Maintain working knowledge according to sponsor’s working instruction, SOPs and other required documents.  Generate and close queries or apply self-evident corrections to the data according to relevant guidelines.  Identify and report protocol violations.  Manual and Patient Profile review, issue queries as per requirement.  Conduct reconciliation of SAEs, send out queries as required and notify relevant Safety Groups of possible issues for their action.  Track and integrate queries.  Interact with site (via mail) as required.  Perform early and final database QC.  Update all relevant tracking system on an ongoing basis.  Inform responsible CDA coordinator of work status regularly.  Keep manager informed about work progress and any issues to avoid surprises.  Maintain a working knowledge and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements and PAREXEL WSOP and study specific procedure.

Clinical Data Analyst I at Parexel International, Jun 2013 - Jun 2015 · 2 yrs 1 mo, Greater Hyderabad Area, Working in all different areas of conduct phase. i.e. Listings, tracker, Query management, subject review... Creating documents, Reconciliation, cross functional team communication.

Senior Clinical Data Co-Ordinator at Lambda Therapeutic Research, Jan 2011 - May 2013 · 2 yrs 5 mos, In lambda working for document preparation and data validation.

Education

Master of biotechnology, Biotechnology, Kadi Sarva Vishwavidyalaya (KSV), Gandhinagar