Manager, CDM (Clinical Data Management)
Bengaluru, India
(Hybrid work model)
Additional locations available
R1491546
Full-Time
Clinical Data Management / Project Management
Hybrid (onsite and remote as per role requirements)
IQVIA is a global leader in clinical research services, commercial insights, and healthcare data intelligence. IQVIA helps life sciences companies accelerate innovation and improve outcomes through data, technology, and advanced analytics.
The Manager, CDM is responsible for overseeing the end-to-end delivery of data management services on single or multi-service projects. The role requires strong leadership to manage timelines, budgets, and quality, ensuring customer satisfaction. The candidate will function as the Data Team Lead (DTL) and provide comprehensive CDM expertise across all project phases.
Collaborate with stakeholders to gather Study Set-Up requirements
Support and oversee validation of new device integrations with minimal guidance
Perform and oversee data cleaning activities, ensuring high-quality and timely deliverables
Ensure all deliverables meet customer expectations and internal quality standards
Ensure timelines and milestones in the Scope of Work (SOW) are met
Lead internal study meetings, sponsor audits, and kick-off meetings
Provide training and mentorship to new team members
Track and manage project progress; identify risks and implement corrective actions
Support implementation of new technologies and database revisions
Collaborate with programming teams to drive process improvements and automation
Maintain compliance with training, eSOPs, and documentation standards
Participate in the development and revision of core SOPs and working instructions
Maintain collaborative communication with line managers and cross-functional teams
Perform other duties as assigned by the Line Manager
Bachelor’s degree in Health, Clinical, Biological, Mathematical Sciences or related field – Required
3–4 years of direct Data Management experience, including 1+ year as CDM project lead – Preferred
Advanced understanding of the drug development lifecycle and clinical research process
Proficient in Microsoft Excel, Word, Outlook, and general data applications
Strong knowledge of clinical data management tools and processes
Exceptional problem-solving, risk assessment, and project tracking capabilities
Strong communication and collaboration skills across cross-functional teams
Experience in leading sponsor interactions, audits, and project delivery
Familiarity with GCP, ICH guidelines, and CDM industry standards
Ability to train, mentor, and support junior team members
Fluent in spoken and written English
IQVIA is an Equal Opportunity Employer and complies with applicable equal employment opportunity legislation in each jurisdiction.
IQVIA combines human science with data science to deliver intelligent insights that help life sciences companies innovate with confidence. Our solutions are powered by deep domain expertise, advanced analytics, and powerful technologies. Learn more at jobs.iqvia.com
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