Department name - Clinical Operations Excellence (COE)
Organization - Novo Nordisk India Pvt Ltd (Affiliate)
Location - Bangalore
Are you ready to shape the future of clinical trial quality at a company reaching more patients than ever before? As our new Clinical Quality & Risk Manager, you will safeguard participant safety and data integrity across our clinical programmes – turning risk insights into action and helping bring life-changing therapies to the people who need them.
Your new role
As Clinical Quality & Risk Manager (CQRM), you will own the CQRM process/framework and be the strategic voice for its implementation and risk management within our Clinical Development Centre (CDC). You will identify emerging risks, design mitigation strategies, and champion a culture of continuous improvement – ensuring every clinical trial we run meets the highest regulatory, ethical and scientific standards.
Day-to-day, your tasks will include:
In Clinical Operations Excellence 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.
You will join Clinical Operations Excellence (COE) within the CDC – the team that sets the standard for how clinical trials are designed, executed and continuously improved. We work shoulder-to-shoulder with trial squads, Global Project Teams, central monitoring and clinical operations leadership, ensuring that quality and risk thinking is embedded into every stage of clinical development. Your contribution will directly strengthen how we protect trial participants and deliver reliable data to advance our pipeline.
Your skills & qualifications
- A Bachelor's degree in Life Sciences, Pharmacy or a related field (Master's preferred), combined with 5+ years of relevant experience in clinical operations or a quality role within the pharmaceutical industry or a CRO
- Proven experience in quality management/assurance with a focus on risk-based quality and quality-by-design, including proficiency in electronic QMS platforms and a strong command of GCP and clinical development
- A solid understanding of data integrity principles, emerging clinical trial technologies, global regulations, and demonstrated expertise in regulatory submission and inspection management
- Demonstrated ability to ensure high-quality execution of clinical trial activities in line with ICH-GCP, regulatory requirements and internal SOPs, supported by strong project management, planning and prioritisation skills
- Excellent interpersonal, negotiation, and problem-solving skills, with the ability to present and communicate with clarity and impact to senior internal stakeholders and external inspectors alike
- Fluency in English, both written and spoken
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.
Contact
To submit your application, please upload your CV online (click on Apply and follow the instructions).
Deadline
3rd July 2026.
Disclaimer
It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organisations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment, or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process.
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.

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic disease and create long-term health.
Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and work to treat, prevent, and even cure diseases that affect millions of lives. Founded in Denmark in 1923, today we employ more than 77,000 people in 80 offices around the world – all united by our bold purpose to drive change to defeat serious chronic diseases. Want to learn more? Visit www.novonordisk.com.
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