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Novo Nordisk Hiring Clinical Data Management

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Novo Nordisk has announced multiple Clinical Data Management openings in Bangalore for experienced life sciences and clinical research professionals. The company is hiring for Associate Clinical Data Facilitator, Associate Senior Clinical Data Management Professional, and Senior Clinical Data Management Professional positions within its Global Business Services (GBS) division.

These opportunities are ideal for candidates with experience in Clinical Data Management (CDM), Electronic Data Capture (EDC), eCOA, GCP, clinical trial operations, vendor management, and regulatory compliance who want to build a long-term career in one of the world’s leading pharmaceutical companies.

If you’re looking for Novo Nordisk Clinical Data Management jobs, Clinical Data Facilitator jobs in Bangalore, or Clinical Data Management careers in India, this recruitment drive offers excellent growth opportunities.


Company Overview

Novo Nordisk is a global healthcare company with more than 100 years of experience developing innovative medicines for chronic diseases. Through its Research & Development organization, Novo Nordisk combines scientific expertise, technology, AI, and clinical research to accelerate drug development while maintaining the highest quality standards.

The Clinical Data Management & Programming team plays a critical role in ensuring accurate, reliable, and regulatory-compliant clinical trial data that supports global regulatory submissions.


Available Positions

1. Associate Clinical Data Facilitator

Experience

  • 2โ€“3 years

Department

  • Data Standards & Integration

Key Responsibilities

  • Manage user access across EDC and eCOA systems
  • Create, modify and deactivate user accounts
  • Configure user management platforms
  • Upload deployment files and user roles
  • Support incident management and troubleshooting
  • Coordinate with global study teams
  • Maintain study versions
  • Perform database lock, study closure and decommission activities
  • Support knowledge-sharing initiatives

2. Associate Senior Clinical Data Management Professional

Experience

  • 2+ years

Key Responsibilities

  • Lead Data Management activities for assigned clinical trials
  • Act as Data Management point of contact
  • Coordinate SDTM, ADaM and TFL deliverables
  • Define data collection strategies
  • Manage trial risks and issue resolution
  • Collaborate with CROs and vendors
  • Ensure GCP compliance
  • Support protocol development and trial planning

3. Senior Clinical Data Management Professional

Experience

  • 3+ years

Key Responsibilities

  • Lead end-to-end Clinical Data Management for global trials
  • Manage complete Data Management project lifecycle
  • Lead Trial Squad activities
  • Coordinate database lock and submission timelines
  • Oversee outsourcing partners and CRO deliverables
  • Drive audit readiness
  • Mentor junior team members
  • Implement process improvements across studies

Educational Qualifications

Candidates should possess any of the following:

  • Bachelor’s Degree in Life Sciences
  • Master’s Degree in Life Sciences
  • Clinical Information Management
  • Computer Science
  • Information Technology
  • Natural Sciences
  • Equivalent relevant qualification

Required Skills

Applicants should have experience with:

  • Clinical Data Management
  • Electronic Data Capture (EDC)
  • eCOA platforms
  • Clinical Trial Operations
  • GCP Guidelines
  • GxP Compliance
  • Good Documentation Practices (GDP)
  • SOP compliance
  • Vendor Management
  • Clinical Data Flow
  • Stakeholder Management
  • Project Coordination
  • Clinical Database Lock
  • SDTM
  • ADaM
  • TFL Deliverables
  • Risk Management
  • English Communication

Preferred Experience

Candidates with experience in:

  • Global Clinical Trials
  • CRO collaboration
  • Clinical Programming
  • Data Standards
  • Regulatory submissions
  • Cross-functional project leadership

will have an added advantage.


Why Join Novo Nordisk?

Working at Novo Nordisk provides access to:

  • Global clinical research projects
  • International collaboration
  • Career progression opportunities
  • Exposure to advanced Clinical Data Management technologies
  • Stable pharmaceutical career
  • Learning and development programs
  • Inclusive work culture
  • Competitive compensation
  • Strong work-life balance
  • Opportunity to contribute to life-changing therapies

Job Location

Bangalore, Karnataka, India


Salary (Estimated)

Based on current industry benchmarks:

RoleEstimated Annual Salary
Associate Clinical Data Facilitatorโ‚น8โ€“12 LPA
Associate Senior CDM Professionalโ‚น10โ€“16 LPA
Senior Clinical Data Management Professionalโ‚น15โ€“24 LPA

Actual compensation depends on experience, skills, and company policies.


How to Apply

Application Link For Associate Clinical Data Facilitator

Application Link For Senior Clinical Data Management Professional

Application Link For Associate Senior Clinical Data Management Professional

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