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Clinical Data Management

3-4 years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Data Management
Location: Pune, India
Job Type: Full Time
Job ID: R1463811

Job Description

IQVIA is seeking a Clinical Data Management professional to manage the end-to-end delivery of data management services for single or multi-service projects. The role involves overseeing the data management process with minimal guidance, ensuring quality deliverables on time and within budget, and providing leadership to the Data Management (DM) team. The individual will perform the role of Data Team Lead (DTL).

Key Responsibilities

  • Study Setup: Gather study setup requirements through communication with relevant stakeholders.

  • Device Integration Validation: Support the validation of new device integrations with minimal guidance.

  • Data Cleaning: Perform regular data cleaning activities to ensure quality and timely deliverables.

  • Quality Standards: Ensure that all deliverables meet customer expectations and quality standards.

  • Timeline Management: Ensure service and quality meet agreed-upon timelines in the contract/Scope of Work (SOW).

  • Training: Support the training of new team members.

  • Meetings: Lead internal study meetings, internal/sponsor audits, and participate in study kick-off meetings and other sponsor meetings.

  • Project Management: Track project progress, identify risks, and take corrective actions to rectify any errors.

  • Technology/Database Implementation: Manage and oversee the implementation of new technology/database revisions.

  • Process Innovation: Work closely with the programming team for process innovation and automation.

  • Compliance: Ensure compliance with training and eSOP reading.

  • Core Operating Procedures: Provide input on developing, revising, and maintaining core operating procedures.

  • Collaboration: Foster communication with line managers and other team members across functions.

  • Additional Duties: Perform other duties as directed by the line manager.

Qualifications

  • Education: Bachelor’s Degree in Pharmacy or equivalent (Preferred).

  • Experience: 3-4 years of direct Data Management experience, including at least 1 year as a CDM project lead (Preferred).

  • Language Proficiency: Fluent in English (Spoken and Written).

  • Skills:

    • Advanced knowledge of computer applications like Microsoft Excel, Word, and Inbox.

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

About IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We connect data, technology, and expertise to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health.


Location: Pune, India
Worker Type: Full Time

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IQVIA is an equal opportunity employer, committed to diversity and inclusion.