Novo Nordisk Hiring Clinical Data Management Professional

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.

Post : Clinical Data Management Professional

Job Description
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.

Candidate Profile
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

Additional Information
Experience : 1+ years
Qualification : MSc/BSc in IT, Natural or Life Sciences
Location : Bangalore, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Research & Development
End Date : 29 May 2026