Clinical Data Management – Project Lead
Locations: Pune, Maharashtra | Bangalore, India
Job Type: Full-Time
Application Deadline: January 24, 2026
Experience Required: 3–4 years (minimum 1 year as CDM Project Lead)
Job ID: R1523107
Company Overview
IQVIA is a global leader in clinical research, data management, and healthcare intelligence. We support pharmaceutical, biotech, and medical device companies in accelerating drug development while ensuring high-quality data integrity. IQVIA combines advanced technology, analytics, and expertise to deliver reliable, compliant, and timely clinical research solutions across the globe.
Role Overview
As a Clinical Data Management Project Lead, you will oversee the end-to-end delivery of data management services for single or multi-service projects. You will ensure quality deliverables are delivered on time, within budget, and in alignment with client expectations. You will also provide leadership, mentorship, and expertise to the Data Management (DM) team while managing project execution, communication, and compliance with industry standards.
Key Responsibilities
Gather study setup requirements through discussions with stakeholders and sponsors.
Oversee validation of new device integrations with minimal guidance.
Perform and supervise data cleaning activities to ensure high-quality, accurate, and timely datasets.
Ensure all deliverables meet expected quality standards and client expectations.
Maintain compliance with timelines, Scope of Work (SOW), and service agreements.
Lead training for new team members and provide ongoing guidance.
Conduct internal study meetings, sponsor audits, kick-off meetings, and other relevant sessions.
Track project progress, identify risks, and implement corrective actions when required.
Support implementation and oversight of new technology, database revisions, and process automation initiatives.
Collaborate closely with programming teams to drive process improvements.
Review, revise, and maintain core operating procedures (SOPs) and working instructions.
Maintain regular communication with the Line Manager and cross-functional teams.
Qualifications & Experience
Education: Bachelor’s degree in Health, Clinical, Biological, Mathematical Sciences, or related field.
Experience: 3–4 years in Clinical Data Management, including at least 1 year as CDM Project Lead preferred.
Skills:
Fluency in spoken and advanced written English.
Proficiency in Microsoft Excel, Word, Outlook, and advanced computer applications.
Strong understanding of the drug development lifecycle and clinical research processes.
Excellent organizational, leadership, and problem-solving skills.
Ability to manage multiple projects, timelines, and priorities efficiently.
Why Join IQVIA
Lead impactful data management projects that influence clinical trial outcomes.
Work with a global leader in clinical research and gain exposure to cutting-edge technology and processes.
Collaborate with expert teams and cross-functional stakeholders to ensure high-quality deliverables.
Opportunities for professional growth, mentorship, and career development in clinical data management.
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