Novo Nordisk India Pvt Ltd

Clinical Data Management Professional

Novo Nordisk India Pvt Ltd
Bengaluru/Bangalore
Not disclosed
Work from OfficeWork from Office
Full TimeFull Time
Min. 1 yearMin. 1 year

Job Description

Clinical Data Management Professional

   

Department: Research & Development 

Company: Novo Nordisk Global Business Services (GBS)


Shape the future of clinical trials by ensuring data quality and integrity that brings life-changing therapies to patients worldwide.

 

Your new role

As a Clinical Data Management Professional, you'll take ownership of critical data management deliverables across clinical trials, ensuring the accuracy and integrity of data that drives evidence-based decisions in drug development. You'll lead DM trial teams, coordinate with global stakeholders, and manage the complete lifecycle of clinical trial data from collection to submission.

Day-to-day your tasks will include:

  • Leading the DM trial team and serving as the primary DM point of contact, co-chairing the Trial Squad to align cross-functional activities
  • Managing Clinical trials, maintaining project plans and coordinating SDTM, ADaM and TFL deliverables to ensure timely database lock
  • Developing and maintaining DM plans, data collection strategies, and key trial documents aligned with protocol requirements and regulatory standards
  • Overseeing DM risk management including RACT, issue resolution, and ensuring audit and inspection readiness
  • Collaborating effectively with CROs and vendors, providing oversight for deliverables managed through the FSO outsourcing model
  • Optimizing trial design through protocol input and defining data collection requirements that balance quality with efficiency
  • Supporting compliance with ICH GCP, regulatory requirements, and internal processes throughout the trial lifecycle

 

Your new department

In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

Within Clinical Data Management & Programming (CDM&P), you'll join a global team dedicated to delivering high-quality clinical trial data that enables evidence-based decision-making. Our culture of continuous learning and innovation drives us to implement new tools, systems, and processes that support the development of life-changing medicines for patients worldwide.

 

Your skills & qualifications

We're looking for a Clinical Data Management Professional who thrives in a dynamic, international environment and brings a strong commitment to data quality and regulatory compliance. You'll bring with you:

  • MSc/BSc in IT, Natural or Life Sciences, or equivalent qualification
  • 1+ years' experience working within clinical data management or equivalent, with a solid understanding of clinical data flow, GCP and regulatory requirements
  • Experience leading trials or small projects in an international setting, demonstrating project management capabilities
  • Strong analytical and data literacy skills, with the ability to solve problems systematically and deliver results through professional expertise
  • Independent, self-driven work style with commitment, persistence and accountability for deliverables
  • Excellent communication and teamwork abilities, with fluency in written and spoken English and the capacity to relate effectively in a multinational environment
  • Results-driven mindset with the ability to manage variable workloads, keep things simple, and continuously adapt to new fit-for-purpose ways of working

 

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

 

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

 

Deadline

29 May 2026. (Applications are reviewed on an ongoing basis.)

 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

 

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Experience Level

Mid Level

Job role

Work location
Work locationBangalore, Karnataka, IN
Department
DepartmentResearch & Development
Role / Category
Role / CategoryPharma & Biotech Research
Employment type
Employment typeFull Time
Shift
ShiftDay Shift

Job requirements

Experience
ExperienceMin. 1 year

About company

Name
NameNovo Nordisk India Pvt Ltd
Job posted by Novo Nordisk India Pvt Ltd

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