Associate Statistical Monitor

Novo Nordisk; Bengaluru; On-site; INR 40,000 - 60,000; Full time

Job summary

A leading global healthcare company in Bangalore is seeking an Associate Statistical Monitor. In this role, you will maintain and operate the Statistical Monitoring function, analyze clinical trial data for irregularities, and collaborate with various teams to ensure compliance. Candidates should have a university degree in life sciences or engineering, with 0-2 years of relevant experience. This position offers a chance to impact clinical trial outcomes and contribute to healthcare innovation.

Qualifications

• 0-2 years of experience in the pharmaceutical industry, ideally with clinical trial data.
• Solid understanding of clinical research and good clinical practice (GCP).
• Basic knowledge of statistical methods and experience with clinical data reporting.

Responsibilities

• Maintain and operate the Statistical Monitoring function.
• Analyze clinical trial data and communicate findings to stakeholders.
• Collaborate with teams to execute Statistical Monitoring activities.

Skills

Analytical skills

Attention to detail

Team-oriented

Proficiency in IT

Flexibility

Education

University degree in life sciences or engineering

Tools

SAS JMP programming

Job description

Novo Nordisk Global Business Services (GBS) India

Department: Centralised Monitoring Unit, CDS GBS - Bengaluru

Are you passionate about ensuring high-quality clinical trial data? Do you have a keen eye for detecting unusual data patterns and a drive to make a meaningful impact on clinical trial outcomes? If so, we invite you to join our team as an Associate Statistical Monitor in Bangalore. Read more and apply today!

The Position

As an Associate Statistical Monitor, you will play a key role in maintaining and operating the Statistical Monitoring function. Your responsibilities will include:

• Operating and maintaining the Statistical Monitoring function to detect unusual data patterns, systematic errors, and potential non-compliance or fraud across trials and projects.
• Collaborating with trial and project teams to plan and execute Statistical Monitoring activities.
• Analyzing clinical trial data to identify irregularities and communicating findings to relevant stakeholders, including trial teams and management.
• Contributing to the development of competencies in Statistical Monitoring by exploring new methods and tools and supporting training initiatives.
• Sharing knowledge and insights to improve the quality of clinical trial data and prevent future occurrences of low-quality data.
• Actively participating in meetings, training sessions, and continuous process improvement initiatives.

Qualifications

We are looking for a motivated individual with the following qualifications:

• A university degree in life sciences or engineering (e.g., B.Sc., MSc, MD) or equivalent.
• 0-2 years of experience in the pharmaceutical industry, preferably with exposure to clinical trial data exploration and visualization.
• A solid understanding of clinical research, GCP, and data flow. Basic knowledge of statistical methods and experience with reporting or publishing clinical/scientific data.
• Proficiency in computer systems and IT, with exposure to SAS JMP programming.
• Strong analytical skills, a quality mindset, and the ability to work independently with statistical monitoring and IT tools.
• Experience working in a regulated industry and familiarity with GxP and drug development guidelines.
• A team-oriented personality with cross-cultural awareness and flexibility.
• A proactive approach to learning and adapting to new situations in a dynamic environment.

About the department

The Centralized Monitoring Unit (CMU) in Bangalore is part of the Clinical Drug Development area. Our department is a perfect blend of skilled medical professionals and technical experts. Medical Reviewers ensure patient safety and protocol compliance, Functional Programmers develop operational visualizations, and Statistical Monitors detect unusual data patterns and compliance issues. Our dynamic and collaborative team is dedicated to making a meaningful impact on clinical trial outcomes. Join us in Bangalore and be part of a team that drives innovation and excellence in clinical research.

Working at Novo Nordisk

Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world, and impacting more than forty million patient lives daily. All of this has made us one of the twenty most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we are working toward something bigger than ourselves, and it is a collective effort. Join us! Together, we go further. Together, we are life changing.

Deadline

15th Jan 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 organizations 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.

“Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.”

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote 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 treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.