Job Title – Senior Data Management Professional Company – Global Business Services, India Department – Clinical Data Management & programming Location – Bangalore Shape the data behind tomorrow's treatments – and help bring life-changing therapies from clinical trials to the patients who need them. Your new role As a Senior Clinical Data Management Professional, you will set the direction and deliver results within your clinical trial(s), ensuring data accuracy, quality, and integrity across the full trial lifecycle. You'll work independently, apply deep subject matter expertise, and play a pivotal role in transforming clinical data into the evidence that supports regulatory submissions and, ultimately, patient access to new therapies. Your key responsibilities will include: <ul style="margin-top:0.0cm;margin-bottom:0.0cm" type="disc"> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Leading the Data Management trial team, acting as the DM point of contact, and co-chairing the Trial Squad</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Planning, executing, and delivering all DM trial activities – from data collection strategy through to database lock and submission deliverables</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Coordinating the CDM&P trial project plan, including SDTM, ADaM, and TFL deliverables, and aligning priorities with trial goals</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Overseeing DM risk management, including RACT ownership and issue resolution with stakeholders</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Ensuring effective collaboration with CROs and vendors, including oversight of deliverables in the FSO outsourcing model</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Driving compliance with ICH GCP, regulatory requirements, and internal processes while maintaining audit and inspection readiness</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Identifying better-practice opportunities, defining process improvements, and mentoring peers through knowledge sharing in relevant forums</li> </ul> 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 R&D, you will join Clinical Data Management & Programming (CDM&P), the team responsible for ensuring the integrity and quality of clinical trial data that underpins every submission we make. Working across therapeutic areas and in close collaboration with statisticians, medical scientists, clinical reporting, and global trial operations, you'll be part of a team that connects rigorous data stewardship directly to patient outcomes. The daily work is performed from your local base, collaborating with colleagues, stakeholders, and projects globally. Your skills & qualifications We're looking for a Senior Clinical Data Management Professional who thrives on complexity and takes pride in delivering high-quality results in a dynamic, international environment. You'll bring with you: <ul style="margin-top:0.0cm;margin-bottom:0.0cm" type="disc"> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">An MSc or BSc in IT, Natural or Life Sciences, or equivalent</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">3+ years of experience working within clinical data management or equivalent, with a good understanding of DM processes, clinical data flow, GCP, and regulatory requirements</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Experience leading trials or projects in an international setting with increasing complexity</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Strong analytical and data literacy skills, combined with excellent project management and coordination abilities</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">A self-driven, results-oriented working style with the ability to handle multiple tasks simultaneously and manage a variable workload</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Open, constructive communication and negotiation skills, with the ability to relate to colleagues in a multinational environment</li> <li style="margin-top:0.0cm;margin-right:0.0cm;margin-bottom:2.0pt;line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Fluency in written and spoken English</li> </ul> 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 28th July 2026. 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.

Senior Clinical Data Management Prof (Bangalore, Karnataka, IN) @ novonord

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