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Functional Programmer

2-4 years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Education: B.Tech/M.Sc/B.Sc 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 - Novo Nordisk (Bangalore, India)

Job Category:
Clinical Development

Location:
Bangalore, India

About the Position:
Novo Nordisk is seeking a skilled Functional Programmer to join their Centralized Monitoring Unit. The ideal candidate will work in a collaborative environment, focusing on data management and generating customized reports for various stakeholders. This role involves programming with SQL/SAS, preparing reports for stakeholders, and contributing to process improvements.

Key Responsibilities:

  • Program Development: Customize existing programs and develop new ones using SQL/SAS, drawing data from systems like COSMOS, DMW, and VEEVA.

  • Report Generation: Generate both standard and customized monitoring reports for stakeholders such as Project Teams, Study Groups, and Management.

  • Ad-Hoc Reporting: Prepare ad-hoc reports related to AESI, data cleaning cycles, and protocol deviations.

  • Report Templates: Develop report templates using data models or mock data for timely development and delivery.

  • Stakeholder Interaction: Chair or conduct Monitoring report meetings, ensuring effective communication and proper documentation.

  • Process Improvement: Provide input to improve processes and training, working collaboratively across teams to enhance site relations.

Qualifications:

Required:

  • B.Tech/M.Sc/B.Sc in Life Science, Computer Science, IT, or related fields.

  • 2-4 years of experience in the pharmaceutical industry, with a minimum of 2 years in clinical data management systems.

  • Proficiency in SAS/SQL and BI tools like PowerBI/Qlik Sense.

  • Expertise in drug development and GxP guidelines.

  • Strong knowledge of computer systems and IT, including validation of computer systems.

Nice to Have:

  • Experience in cross-border collaboration.

  • Strong communication and presentation skills.

  • Ability to mentor and supervise.

  • Project management experience.

  • Technical problem-solving skills for data challenges.

About the Department:
The Centralized Monitoring Unit is dedicated to supporting Risk-Based Quality Management (RBQM) across trial portfolios. The team is focused on creating standard and customized monitoring reports, collaborating closely with stakeholders to improve processes and enhance site relations.

Working at Novo Nordisk:
Novo Nordisk is a global leader in healthcare, focusing on chronic diseases, particularly diabetes. The company’s success relies on the collective potential and collaboration of its employees, impacting millions of patients worldwide. Novo Nordisk strives to create an inclusive culture and recognizes the importance of diverse perspectives to drive innovation.

Application Process:
To apply, please upload your CV and motivational letter through the online application portal.

Deadline for Applications:
April 18, 2025

Disclaimer:
Be cautious of fraudulent job offers. Novo Nordisk does not extend unsolicited job offers or request payment during the recruitment process.

Commitment to Diversity:
Novo Nordisk is committed to creating an inclusive culture that celebrates diversity and strives to be the best company for the world, not just the best in the world.