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Manager, Cdm

3–4 years years
Not Disclosed
10 Aug. 29, 2025
Job Description
Job Type: Hybrid Education: Bachelor’s degree in Health, Clinical, Biological, Mathematical Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

ob Title

Manager, CDM (Clinical Data Management)


Location

Bengaluru, India
(Hybrid work model)
Additional locations available


Job ID

R1491546


Job Type

Full-Time


Category

Clinical Data Management / Project Management


Work Model

Hybrid (onsite and remote as per role requirements)


Company Overview

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.


Role Summary

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.


Key Responsibilities

  • 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


Qualifications

  • 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 leadPreferred


Skills & Proficiencies

  • 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


Languages

  • Fluent in spoken and written English


Equal Opportunity Statement

IQVIA is an Equal Opportunity Employer and complies with applicable equal employment opportunity legislation in each jurisdiction.


About IQVIA

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