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Functional Programmer

2-4 years
Not Disclosed
10 April 9, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Functional Programmer

Category: Centralized Monitoring
Department: Centralized Monitoring Unit
Location: Not specified (assumed India/global office)


Position Summary

Novo Nordisk is looking for a Functional Programmer to join the Centralized Monitoring Unit and support Risk Based Quality Management (RBQM) across clinical trial portfolios. The role involves programming monitoring reports using tools like SQL/SAS and integrating data from systems such as COSMOS, DMW, and VEEVA.


Key Responsibilities

  • Understand stakeholder requirements for monitoring reports and create technical specifications.

  • Program new or modify existing reports using SQL, SAS, or other relevant languages.

  • Integrate data from platforms like COSMOS, DMW, and VEEVA to generate meaningful outputs.

  • Produce standard, custom, and ad-hoc reports for teams such as Project Management, Study Groups, and Regulatory bodies.

  • Prepare report templates using mock data for timely delivery of reporting tools.

  • Conduct and lead report review meetings, ensuring proper documentation and understanding.

  • Suggest and support process improvements, training sessions, and cross-team collaboration.

  • Help enhance site relations through transparent, actionable reporting.


Qualifications

Required

  • B.Tech/M.Sc/B.Sc in Life Sciences, Computer Science, IT, or a related domain.

  • 2–4 years of experience in the pharmaceutical industry.

  • At least 2 years of hands-on experience in clinical data management systems.

  • Expert-level understanding of IT systems, especially in a GxP-regulated environment.

  • Proficiency in at least one programming language (SAS, SQL) and BI tools like PowerBI or Qlik Sense.

  • Sound knowledge of drug development, regulatory guidelines, and clinical workflows.

Preferred

  • Experience in cross-functional collaboration across regions.

  • Strong presentation and communication skills.

  • Ability to mentor or supervise team members.

  • Project management skills.

  • Proactive problem-solving and solution identification in a data-driven environment.


About the Department

The Centralized Monitoring Unit supports Novo Nordisk’s Risk Based Quality Management (RBQM) by delivering reports and dashboards that improve decision-making, safety, and clinical trial monitoring efficiency. The department values collaboration, innovation, and a continuous improvement mindset.


About Novo Nordisk

Novo Nordisk is a global leader in healthcare, with a 100-year history of delivering innovative treatments for diabetes, obesity, and other serious chronic diseases. With over 72,000 employees worldwide, the company strives to create life-changing careers through purposeful innovation and a strong commitment to patient well-being.


Application Instructions

Submit your CV and motivational letter via the official Novo Nordisk careers page.

Deadline: 18th April 2025


Disclaimer

Be aware of fraudulent job offers. Novo Nordisk does not request fees, personal purchases, or training payments during recruitment. All legitimate offers are made through the official Novo Nordisk recruitment platform.


Inclusion Commitment

Novo Nordisk is dedicated to fostering a diverse and inclusive culture. The organization believes that being the best company for the world starts with empowering its diverse employees, supporting their ideas, and enabling meaningful contributions.