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Clinical Data Management Professional

Novo Nordisk
Novo Nordisk
1-5 years
preferred by company
Bangalore, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding

Clinical Data Management Professional

Location: Bengaluru, Karnataka, India
Company: Novo Nordisk Global Business Services (GBS)
Job Type: Full-Time
Work Mode: Hybrid / Onsite (As Per Business Requirement)
Industry: Clinical Research | Clinical Data Management | Pharmaceutical | Life Sciences | Data & AI
Department: Research & Development | Clinical Data Management & Programming (CDM&P)
Experience Required: 1–5+ Years (Freshers Not Eligible)
Qualification Required: B.Sc / M.Sc in Life Sciences, Natural Sciences, IT, or Equivalent

Job Overview

Novo Nordisk is hiring a Clinical Data Management Professional for its Global Business Services team in Bengaluru. This opportunity is ideal for professionals with expertise in clinical data management, clinical trial data operations, SDTM, ADaM, TFL coordination, database lock management, regulatory compliance, CRO oversight, and clinical research data governance.

The selected candidate will play a critical role in managing end-to-end clinical trial data management activities, ensuring high-quality, audit-ready, and submission-compliant data that supports evidence-based drug development decisions.

This role is ideal for professionals looking to grow in clinical data management, pharmaceutical research operations, clinical trial data governance, and global drug development programs.

Job Responsibilities

Clinical Data Management Leadership

  • Lead clinical data management trial teams for assigned studies.
  • Serve as the primary Clinical Data Management (CDM) point of contact for trial activities.
  • Co-chair trial squads and align cross-functional data management deliverables.
  • Drive operational coordination across clinical development stakeholders.

Clinical Trial Data Lifecycle Management

Manage end-to-end clinical trial data processes including:

  • Data collection strategy planning
  • Clinical database oversight
  • Data validation
  • Query management support
  • Database lock planning
  • Final clinical data readiness
  • Submission data coordination

Ensure high data integrity throughout the clinical trial lifecycle.

SDTM, ADaM & TFL Coordination

Coordinate and support key clinical programming deliverables including:

  • SDTM (Study Data Tabulation Model)
  • ADaM (Analysis Data Model)
  • TFLs (Tables, Figures, and Listings)

Ensure timely alignment for database lock and downstream submission milestones.

Data Management Planning & Documentation

Develop and maintain critical trial documentation including:

  • Data Management Plans
  • Data collection strategies
  • Clinical trial data workflows
  • Protocol-aligned documentation
  • Regulatory-compliant data deliverables

Risk Management & Inspection Readiness

  • Oversee clinical data risk management activities.
  • Manage:
    • RACT processes
    • Issue escalation
    • Risk mitigation
    • Data quality governance
  • Ensure audit and inspection readiness for assigned trials.

CRO & Vendor Oversight

  • Collaborate with CROs and external vendors supporting clinical data activities.
  • Provide oversight for outsourced deliverables under the FSO model.
  • Ensure vendor quality, timeline compliance, and operational alignment.

Protocol & Trial Design Support

  • Contribute to protocol development from a data management perspective.
  • Define efficient and compliant data collection requirements.
  • Optimize trial data design balancing quality, operational efficiency, and compliance.

Regulatory Compliance

Ensure adherence to:

  • ICH GCP guidelines
  • Clinical research regulatory standards
  • Internal pharmaceutical data governance processes
  • Global clinical trial compliance requirements

Cross-Functional Collaboration

Work closely with:

  • Clinical Operations
  • Biostatistics
  • Programming teams
  • Medical stakeholders
  • CRO partners
  • Regulatory functions
  • Global trial leadership teams

About the Department

The Clinical Data Management & Programming (CDM&P) team at Novo Nordisk supports global clinical development programs by delivering high-quality clinical trial data that enables evidence-based drug development and regulatory decision-making.

The broader Research & Development organization combines scientific innovation, advanced technology, AI tools, and human expertise to accelerate the development of transformative therapies for patients worldwide.

Educational Qualification

Candidates must have:

  • B.Sc
    OR
  • M.Sc
    OR equivalent qualification in:
    • Life Sciences
    • Natural Sciences
    • Information Technology
    • Clinical Research
    • Biotechnology
    • Biomedical Sciences