Job Title: Senior Data Strategist (Principal Data Manager)
📍 Location: Bengaluru, India | Hybrid
🏢 Work Type: Full-time
📄 Job Code: R1501324
Job Overview
The Senior Data Strategist (Principal Data Manager) will oversee end-to-end data operations for global clinical trials and laboratory studies, ensuring high-quality, clean, and analyzable databases. This role provides leadership to the CDM team, manages customer relationships, drives process improvement, and delivers data management excellence across multiple complex projects.
Key Responsibilities
Leadership & Project Oversight
Serve as Data Team Lead (DTL) for 6–10 global clinical trials or 40+ complex central laboratory studies.
Provide leadership, guidance, and mentorship to the CDM team.
Act as a back-up for Data Team Lead or Data Operations Coordinator (DOC) as required.
Represent CDM in customer negotiations on complex timelines, budgets, and deliverables.
Customer & Business Development
Manage CDM customer relationships, ensuring satisfaction and delivery excellence.
Lead business development presentations and capabilities discussions with clients.
Provide expert input during bid defense meetings and project negotiations.
Operational Management
Oversee project delivery through the full data management lifecycle, from start-up to database lock.
Manage:
Project timelines and milestones
Quality control and issue resolution
Resource allocation
Budget/SOW (scope of work) justification and management
Ensure adherence to SOPs, work instructions, and regulatory standards.
Technical Expertise & Innovation
Act as a Subject Matter Expert (SME) in specialized data management areas (e.g., SAE reconciliation, central laboratory data, therapeutic areas, or new technology).
Lead process improvement initiatives and implementation of new technologies/tools.
Present at professional conferences and publish in industry journals.
Team Development
Mentor team members to develop clinical data management expertise.
Manage best practice teams or focus groups within CDM.
Support training initiatives and continuous improvement efforts.
Qualifications
Education:
Bachelor’s degree in Clinical, Biological, or Mathematical Sciences, or Nursing qualification (required).
Equivalent combination of education, training, and experience may be considered.
Experience:
Minimum 5 years’ experience in Clinical Data Management (CDM).
Proven ability to manage multiple large global projects (including trials with >1000 patients).
Demonstrated experience in customer negotiations, bid defense, and client management.
Strong knowledge of CDM processes, SOPs, and specialized data management skills.
Skills:
Excellent organizational, leadership, and project management skills.
Strong communication and relationship-building abilities.
Comprehensive understanding of clinical drug development processes.
Ability to resolve complex issues independently and provide expert solutions.
About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. We accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
🌐 Learn more: IQVIA Careers
✅ Apply Now
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