Senior Data Team Lead (Clinical Data Management)
Location: Bengaluru, India
Job Type: Full-Time
Reference ID: R1529803
Company: IQVIA
About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The organization partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development, ensure regulatory compliance, and improve patient outcomes worldwide.
This role offers an opportunity to lead end-to-end Clinical Data Management (CDM) delivery for complex global trials within a high-performance, regulatory-driven environment.
Role Overview
The Senior Data Team Lead (Sr. DTL) is responsible for independently managing full lifecycle clinical data management services across single or multi-service projects, including large global programs. This leadership role ensures high-quality data deliverables are completed on time, within budget, and in compliance with Good Clinical Practice (GCP) and regulatory requirements.
The Sr. DTL serves as the primary client contact for data management activities and may also act as Program Lead, Customer Site Manager, Subject Matter Expert (SME), or Project Manager for data-only services.
Key Responsibilities
Client & Stakeholder Management
Serve as the primary point of contact for customers on all data management deliverables.
Lead negotiations related to timelines, budgets, processes, and resources.
Maintain strong client relationships and ensure contractual obligations are met.
Provide escalation support for complex data or operational issues.
Global Clinical Data Management Leadership
Manage multiple large-scale global clinical trials or programs through the full data management lifecycle.
Provide senior oversight and mentoring to Data Team Leads (DTLs).
Oversee Data Management Plans (DMPs), review and approve documentation.
Ensure compliance with GCP, regulatory guidelines, SOPs, and internal policies.
Project & Service Delivery Management
Ensure milestones are achieved within agreed timelines and quality standards.
Coordinate with Data Operations Coordinators (DOCs), project managers, and functional leads.
Proactively implement quality management plans across projects.
Identify root causes of service issues and implement corrective and preventive actions.
Optimize workflows and drive continuous process improvements.
Financial & Business Oversight
Manage budgets and Statements of Work (SOW).
Review financial reports, revenue recognition, and invoicing processes.
Identify and manage out-of-scope activities and change orders.
Participate in bid defense meetings and pricing discussions.
Subject Matter Expertise & Leadership
Serve as SME in specialized CDM processes or technologies.
Lead development and implementation of new tools or technologies.
Mentor and train junior DTL staff in clinical data management best practices.
Contribute to global or local best practice initiatives.
Present lessons learned in CDM workshops or industry forums.
Required Experience
Minimum 5+ years of direct Clinical Data Management (CDM) experience.
At least 3+ years of experience as a CDM Project Lead or Data Team Lead preferred.
Proven experience managing large global trials (minimum 1,000+ patients) across the full data management lifecycle.
Demonstrated expertise in:
SAE reconciliation
External vendor data reconciliation
Local laboratory data management
Advanced DM processes and technologies
Experience handling complex customer negotiations and bid defense meetings independently.
Strong knowledge of GCP guidelines and global regulatory requirements.
Comprehensive understanding of the clinical drug development process.
Educational Qualifications
Bachelor’s degree in Health Sciences, Clinical Sciences, Biological Sciences, Mathematical Sciences, or related field required.
Core Competencies
Advanced clinical data management lifecycle expertise
Strong project and financial management skills
Customer relationship and stakeholder engagement expertise
Risk assessment and escalation management
Regulatory compliance and GCP adherence
Leadership, mentoring, and team development capabilities
Excellent organizational and problem-solving skills
Why Join IQVIA Clinical Data Management
Lead global, large-scale clinical data programs.
Work within a regulatory-compliant, high-performance environment.
Gain exposure to enterprise-level customer management and strategic decision-making.
Contribute to innovative clinical development initiatives that impact global healthcare.
IQVIA maintains strict integrity standards in its recruitment process and enforces a zero-tolerance policy toward candidate fraud or misrepresentation. All submitted information must be accurate and complete.
Advance your leadership career in Clinical Data Management with IQVIA.
Explore more global clinical research and pharmaceutical leadership opportunities at The Pharma Daily.
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