Associate Functional Programmer

Novo Nordisk A/S; Bengaluru; On-site; INR 1,500,000 - 2,200,000; Full time

Job summary

Novo Nordisk A/S in Bengaluru seeks an Associate Functional Programmer to build and maintain monitoring reports supporting Risk-Based Quality Management for its clinical trial portfolio. You’ll collaborate with cross-functional stakeholders to turn complex data into actionable insights ensuring trial quality and patient safety.

The role involves developing programs using CMP, Qlik Sense, SQL, SAS, JMP, Power BI, Databricks, Python, and R, and delivering ad-hoc reports while contributing to data

Qualifications

• Master's or Bachelor's degree in Life Sciences, Computer Science, Information Technology, Clinical Information Management, or equivalent.
• 1–3 years of pharma industry experience, including 1–2 years in clinical data management systems, bioinformatics, or as a CRA.
• Proficiency in at least one programming language (SAS, SQL, Python, or R) and ability to solve data challenges.
• Familiarity with drug development, GxP, and computer system validation.
• Strong analytics and English communication, collaboration in diverse teams.

Responsibilities

• Generate standard and customised monitoring reports to support Risk-Based Quality Management across trials.
• Develop or customize programs using CMP, Qlik Sense, SQL, SAS, JMP, Power BI, Databricks, Python, and R.
• Interpret stakeholder requirements and draft detailed report specifications.
• Produce ad-hoc reports for AESI, data cleaning, protocol deviations, and site data entry statuses.
• Create validation docs, peer review reports, and design report templates from data models.
• Attend monitoring report meetings and track action items and data availability.

Skills

Programming basics

Analytical skills

English communication

Education

Life Sciences/CS/IT degree

Tools

Central Monitoring Platform (CMP)

Qlik Sense

SQL

SAS

JMP

Power BI

Databricks

Python

R

Job description

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Company – Novo, Global Business Services (GBS)
Department – Research & Development
Location – Bangalore, India

Turn clinical data into meaningful insights that help bring life-changing therapies to patients faster. In this role, you'll develop monitoring reports that directly support the quality and safety of clinical trials across our global portfolio.

Your new role

As an Associate Functional Programmer, you will generate and maintain monitoring reports that support Risk-Based Quality Management (RBQM) across Novo's clinical trial portfolio. You'll work closely with cross-functional stakeholders to translate complex data into actionable insights that safeguard trial quality and patient safety.

Your key responsibilities will include:

• Generating standard and customised monitoring reports (Trial, Central, Medical Monitoring, and Risk Indicator reports) to support RBQM across the trial portfolio
• Developing new programs or customising existing ones using tools such as Central Monitoring Platform (CMP), Qlik Sense, SQL, SAS, JMP, Power BI, Databricks, Python, and R – integrating data from multiple sources
• Understanding stakeholder requirements and preparing detailed specifications for report development
• Producing ad-hoc reports (e.g., AESI, Data Cleaning cycles, Protocol deviations, Site Data Entry statuses, Subject lists) for various stakeholder groups
• Creating validation documentation, conducting peer reviews of programs and reports, and designing report templates using data models or mock data
• Participating in monitoring report meetings, recording minutes, providing input on data availability, and following up on action items

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.

You will be based in our Global Business Services centre in Bengaluru, working as part of the Trial Monitoring & Reporting team. The team plays a critical role in ensuring the quality and integrity of clinical trial data through robust reporting frameworks. You'll collaborate daily with colleagues at headquarters and across our global clinical operations, with opportunities for international travel for training and stakeholder engagement.

Your skills & qualifications

We're looking for a detail-oriented and curious Associate Functional Programmer who thrives in a collaborative, data-driven environment. You'll bring with you:

• A Master's or Bachelor's degree in Life Sciences, Computer Science, Information Technology, Clinical Information Management, or an equivalent qualification
• 1–3 years of experience in the pharmaceutical industry, preferably including 1–2 years within clinical data management systems, bioinformatics, or as a Clinical Research Associate
• Basic proficiency in at least one programming language such as SAS, SQL, Python, or R, with the ability to identify technical solutions for data challenges
• Familiarity with drug development processes, basic medical terminology, GxP guidelines, and computer system validation processes
• Strong analytical skills with an aptitude for data analytics and statistical concepts, combined with proficiency in written and spoken English and the ability to collaborate effectively in a diverse, multi-cultural environment

Working at Novo

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.

Deadline

30th October 2026.

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