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Associate Clinical Data Manager

2+ 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

Job Title: Associate Clinical Data Manager
Location: Kochi, India
Job ID: R1475595
Job Type: Full Time


Job Overview:

The Associate Clinical Data Manager will act as a Lead Data Manager on multiple data management projects, ensuring the delivery of high-quality data to clients. This role involves direct coordination with sponsors, cross-functional teams, and other global sites to support clinical data lifecycle activities from setup through final delivery.


Responsibilities:

  • Study Setup & Database Design:

    • Gather setup requirements from stakeholders.

    • Perform database design and validation to ensure optimal data collection structures.

  • Device Integration & Data Cleaning:

    • Validate new device integrations for data capture.

    • Conduct regular data cleaning to meet quality and delivery standards.

  • Project Management & Stakeholder Coordination:

    • Lead internal meetings, audits, and sponsor kick-off sessions.

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

  • Process Improvement:

    • Collaborate with programming teams for process automation and innovation.

    • Manage development and upgrades of database technologies.

  • Team Support & Training:

    • Train and support new joiners in processes and tools.

    • Maintain compliance with eSOPs and ongoing training requirements.

  • Quality Assurance:

    • Ensure all deliverables align with expected quality standards and client expectations.

    • Contribute to the development and revision of core procedures and instructions.


Qualifications:

  • Education: Master's Degree in Science / Bachelor's in Pharmacy or equivalent preferred.

  • Experience: Experience in clinical data management or a related field is desirable.

  • Skills:

    • Advanced proficiency in Microsoft Office applications.

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

    • Excellent written and verbal English communication skills.

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


About IQVIA:
IQVIA is a global leader in clinical research and healthcare intelligence, dedicated to accelerating innovation and improving outcomes in the life sciences industry.

Visit Careers at IQVIA


Equal Opportunity Employer:
IQVIA provides equal employment opportunities without regard to race, color, religion, sex, national origin, disability, veteran status, or any other protected status.