Company – Global Business Services, India Department – Clinical Data Management Location – Bangalore Are you passionate about supporting clinical trial technologies and ensuring smooth access to critical clinical data systems? Do you thrive in a collaborative, global environment where quality, compliance, and innovation are at the heart of everything you do? If so, you could be our next User Access & Clinical Data Systems Associate at Novo Nordisk. Your new role As a Clinical Data Insight Analyst, you will play an important role in supporting the administration and maintenance of clinical data management systems across global clinical trials. You will be responsible for managing user access, configuring systems, supporting end-users, and ensuring compliance with applicable processes and regulatory requirements. In this role, you will collaborate with stakeholders across Clinical Data Management, Clinical Operations, Biostatistics, Digital Innovation, and external vendors to deliver efficient and compliant solutions that support clinical trial execution. Your key responsibilities will include: <ul> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Managing site and user access across clinical data management systems such as EDC and eCOA platforms.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Creating, maintaining, and deactivating user accounts for internal and external stakeholders.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Performing configuration activities within user management tools and Veeva systems.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Managing rights, roles, study setup activities, and study closure/decommissioning processes.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Supporting incident management and resolving user access and system-related queries.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Ensuring documentation is maintained in accordance with company standards, SOPs, GCP, GDP, and GxP requirements.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Collaborating with cross-functional and global teams to meet project timelines and operational goals.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Contributing to process improvements and sharing best practices across teams and functions.</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 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 <ul> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Bachelor's or Master's degree in Life Sciences, Computer Science, Information Technology, Clinical Information Management, or a related field.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">2–3 years of experience within the pharmaceutical, biotechnology, clinical research, or healthcare industry.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Experience working with Clinical Data Management systems, user access management, vendor systems, or related platforms.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Knowledge of clinical trial processes and GxP requirements within drug development.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Strong understanding of computer systems, applications, and IT processes.</li> <li style="line-height:14.0pt;font-size:12.0pt;font-family:verdana, geneva, sans-serif;color:black">Excellent written and verbal communication skills in 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. 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.

Associate Senior Clinical Data Insights Analyst (Bangalore, Karnataka, IN) @ novonord

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