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Functional Programmer

2-3 years
Not Disclosed
10 July 21, 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

 

Functional Programmer – Clinical Trials | Novo Nordisk | Bangalore

Job Summary:
Novo Nordisk is hiring a Functional Programmer to support centralized monitoring of global clinical trials. Based in Bangalore, this role focuses on delivering high-quality data visualizations and reports using SAS, SQL, Power BI, and Python for risk-based quality monitoring (RBQM). Ideal for professionals with 3+ years in pharma or life sciences and a strong background in clinical data handling and IT.


Key Responsibilities:

  • Generate standard and custom trial monitoring reports using SAS, SQL, Python, Power BI, and related tools (e.g., Qlik Sense, Clue Point).

  • Align reports with Risk-Based Quality Monitoring (RBQM) requirements and stakeholder needs.

  • Prepare, maintain, and peer-review reporting documentation.

  • Perform rigorous quality checks to ensure data accuracy and compliance.

  • Conduct trial monitoring meetings and track requests.

  • Mentor and train new team members and contribute to onboarding and documentation efforts.

  • Support process enhancements and resource planning.


Required Skills & Qualifications:

  • Bachelor's or Master's in Life Sciences, Computer Science, IT, Clinical Data Management, or related fields.

  • 3+ years of experience in the pharma/life sciences industry, with 2+ years in clinical data management or clinical research.

  • Strong command of programming tools like SAS, SQL, Power BI, Python, and knowledge of tools like JSL, R-Shiny, NLP is a plus.

  • Solid understanding of GxP, ICH-GCP, and international drug development regulations.

  • Experience in project management, mentoring, and cross-functional collaboration.

  • Proficient in medical and clinical terminology.


Perks & Benefits:

  • Work with one of the world’s top 20 companies by market cap.

  • Exposure to global clinical development portfolios.

  • Career growth in a dynamic and inclusive work environment.

  • Access to cutting-edge tools and training resources.

  • Opportunity to contribute to the development of life-changing therapies.


Company Description:

Novo Nordisk is a global healthcare leader with over 100 years of legacy in addressing chronic diseases like diabetes, obesity, and rare conditions. With over 72,000 employees globally, we focus on innovation, collaboration, and long-term health solutions impacting over 40 million lives daily.


Work Mode: On-site – Bangalore, India


Call-to-Action:
Ready to help shape the future of healthcare? Apply now to join Novo Nordisk’s dynamic Centralised Monitoring Unit and make a difference in global clinical development. Deadline: 25th July 2025