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Manager, Cdm

3-4 years
Not Disclosed
10 Sept. 17, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life 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

Job Title: Manager, Clinical Data Management (CDM)

📍 Location: Bengaluru, India | Hybrid
🏢 Work Type: Full-time
📄 Job Code: R1491546


Job Overview

The Manager, CDM will be responsible for the end-to-end delivery of data management services for single or multi-service projects. The role involves ensuring quality deliverables are completed on time, within budget, and to customer satisfaction. This position also provides leadership, oversight, and expertise to Data Management (DM) teams across study setup, execution, and closeout, while acting as the Data Team Lead (DTL).


Key Responsibilities

  • Study Setup & Planning

    • Gather study setup requirements through stakeholder discussions.

    • Provide oversight for validation of new device integrations.

  • Data Management & Quality Oversight

    • Supervise and perform data cleaning activities to ensure accuracy, compliance, and timely sponsor deliverables.

    • Ensure deliverables meet quality standards and customer expectations.

    • Track and manage project progress, identify risks, and implement corrective actions.

  • Leadership & Collaboration

    • Act as Data Team Lead (DTL) on projects.

    • Lead internal study meetings, audits, and sponsor meetings (e.g., study kick-offs).

    • Support training of new joiners and mentor team members.

    • Collaborate with cross-functional teams, programming, and process innovation groups.

  • Technology & Process Improvements

    • Oversee implementation of new technology or database revisions.

    • Contribute to process innovation, automation, and continuous improvement.

    • Review and provide input on operating procedures and work instructions.

  • Compliance & Documentation

    • Ensure compliance with required trainings, eSOPs, and regulatory standards.

    • Provide expert review in SOP development and revision.

    • Maintain clear, collaborative communication with line managers and stakeholders.

  • Other Duties

    • Perform additional tasks as directed by the line manager.


Qualifications

  • Education:

    • Bachelor’s degree in health, clinical, biological, mathematical sciences, or related field (required).

  • Experience:

    • 3–4 years of direct Data Management experience.

    • Minimum 1 year as a CDM project lead (preferred).

  • Skills & Knowledge:

    • Advanced understanding of the drug development lifecycle and clinical research process.

    • Strong command of Microsoft Excel, Word, and related tools.

    • Excellent English communication skills (spoken and written).

    • Strong organizational, leadership, and problem-solving skills.


About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide.

🌐 Learn more: IQVIA Careers


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