Clinical Data Insights Analyst

Novo Nordisk India Pvt Ltd; Bengaluru; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Novo Nordisk India Pvt Ltd in Bangalore is seeking a Clinical Data Insights Analyst to drive data review and quality for clinical trials. You will manage risk-based data review activities, raise and close queries with EDC/CDMS, and communicate insights through visualizations to support decision making.

Ideal candidates have MSc/BSc in life sciences or medicine, plus experience in Clinical Data Management. Strong English communication and cross-cultural collaboration are expected within a global

Qualifications

• MSc/BSc in Natural/Life Science, medicine, or a CS degree with relevant experience.
• Preferably 2+ years in Clinical Data Management within pharma or drug development.
• Experience with clinical trial methodology and regulatory requirements (GCP) is valued.

Responsibilities

• Plan, coordinate and execute data reviews, including risk-based data review.
• Create data review specifications and collaborate with developers for tools/ UAT deployment.
• Review clinical data across formats for completeness, accuracy and integrity.
• Raise, review and close queries with EDC/CDMS and ensure data is corrected as needed.
• Communicate findings with visualizations to support trial decisions.

Skills

Data visualization

Communication

Teamwork

Analytical thinking

English proficiency

Education

MSc/BSc Natural/Life Science

Medicine degree

Computer Science degree

Tools

Clinical data systems

GCP knowledge

Job description

Clinical Data Insights Analyst Company – Novo Nordisk, Global Business Services Department – Research & Developement Location – Bangalore Turn clinical data into insights that shape the future of patient care. Your new role As a Clinical Data Insights Analyst, you will be the Data Management (DM) Trial Partner within the trial DM team. Your key responsibilities will be planning and executing data review, including risk-based data review, implementing associated risk management and mitigation activities, and ensuring quality data for analysis and submission.Day-to-day your tasks will include: Planning, coordinating, and assessing risks associated with data review by using various tools and technologies and applying risk-based data management approaches Creating specifications for data review tools, including reports and visualizations, and collaborating with programmers to ensure successful setup, UAT, and deployment Review clinical data in various database formats, datasets, listings, reports, visualizations, and analytics for completeness, accuracy, and integrity Raise, review and close of queries with EDC/CDMS ensuring that data is reviewed and corrected as required by qualified site staff Proactively own and independently drive all data review under CDR purview and effectively communicate data findings including visualizations with clear explanations. Use data visualisation methods to review and understand data to support trial partners in making operational decisions Analyzing data patterns and trends to detect anomalies Communicating data review findings and trending analysis to stakeholders through effective visualizations, supporting operational decisions, and identifying site/CRA training needs Maintaining strong working relationships with Data Management trial partners and other stakeholders to successfully achieve data review deliverables according to trial timelines Preparing for and participating in audits and inspections, maintaining trial documentation, and ensuring proper archival on an ongoing basis Participating in process and toolkit improvement projects as required to support the evolution of data review and cleaning processesVerify data review completion with DM trial partners before database lock

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 Insights Analyst who thrives in a data-driven environment and enjoys turning complex information into meaningful insights. You'll bring with you: MSc/BSc in Natural/Life Science, comparable degree in medicine, or a degree in computer science with equivalent professional experience Preferably 2+ years of Clinical Data Management experience, with the majority within the pharmaceutical industry or drug development Knowledge of clinical trial methodology and preferably basic understanding of GCP and relevant regulatory requirements Experience working with clinical systems used in drug development and understanding of clinical data processing and flow Fluent written and verbal English with effective communication, presentation, and negotiation skillsTeam-oriented personality with high flexibility, cross-cultural awareness, and ability to build and maintain solid internal networks Ability to adjust quickly to new situations in a continuously developing environment, acting in accordance with the Novo Nordisk Way Working at Novo Nordisk

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. In R&D, your analytical skills and attention to detail directly contribute to breakthrough therapies that reach millions of patients. Here, you'll work alongside passionate colleagues who value both scientific rigor and diverse thinking, creating an environment where your insights make a tangible difference to patients worldwide.

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 21st September 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.