Senior Clinical Programmer

Novo Nordisk India Pvt Ltd; Bengaluru; In loco; INR 1.800.000 - 3.200.000; Tempo pieno

Descrizione del lavoro

Novo Nordisk India Pvt Ltd in Bengaluru is seeking a hands-on data/AI expert to lead projects on AI/ML for clinical data, deploy models, and build scalable data pipelines. You will implement GenAI apps, manage data from diverse sources, and deliver actionable insights to cross-functional teams.

The role emphasizes DevOps/MLOps, SQL/Python/R, and communication in a global environment, with collaboration across Clinical Operations and IT. 4–6 years in pharma data is preferred.

Competenze

• 4-6 years of experience in the pharmaceutical industry.
• Knowledge of and experience with AI/ML, CI/CD pipelines, Python and R.
• Experience with data visualisation tools such as Tableau or Power BI.
• A good understanding of databases and SQL.
• Understanding of clinical protocols, CRF standards, InForm terminology and EDC data structure.
• Profound knowledge of GxP and drug development guidelines.
• Experience in project management, collaboration and presentation.
• Fluent written and spoken English, cultural awareness and the ability to work in a diverse, global environment.
• A proactive, quality-minded approach, with strong analytical skills and the ability to plan your work.
• Useful, but not essential: Knowledge of clinical development and basic medical terminology.
• 2+ years of experience within clinical data management systems.
• Experience with AWS and REST or other APIs.

Mansioni

• Own projects and work with minimal supervision, following SOPs and policies.
• Build, validate and deploy deep learning models for patient stratification, endpoint prediction and data anomaly detection.
• Manage model lifecycle including versioning, drift monitoring and retraining.
• Implement Generative AI applications, including LLMs and RAG systems, to automate document processing and query clinical databases.
• Build automated ETL pipelines on Azure DevOps and Databricks to harmonise complex clinical data sources.
• Apply DevOps and MLOps practices, CI/CD pipelines, and advanced Python and SQL for reliable production apps.
• Program, review and update complex clinical reports from documented requirements, using SQL, SAS, Python, R and CI/CD pipelines.
• Deliver on time, solve problems during a trial, and provide actionable insights to stakeholders.
• Support leads in coordinating reporting with external partners.
• Design, develop and maintain dashboards and reusable visualization components.
• Support tools for data collection, transformation and analysis, test and debug end to end, and improve older databases.
• Create training materials and share learnings.
• Keep documentation up to date and work with SMEs to interpret trial data.
• Act early on concerns to protect data accuracy and quality, and support data review training.
• Lead or support small projects and provide input to improve standards and processes.

Conoscenze

AI/ML

CI/CD pipelines

Python

R

Tableau

Power BI

Databases

SQL

GxP

Drug development

Project management

Stakeholder management

English fluency

JavaScript

AngularJS

Formazione

Life Science degree

Computer Science degree

Information Technology degree

Strumenti

Azure DevOps

Databricks

SAS

REST APIs

JavaScript

AngularJS

Descrizione del lavoro

What you’ll bring

You know clinical data, you can program, and you can explain what the data shows. You are a hands-on expert with a passion for advanced AI and for clinical trial data. A Master's or Bachelor's degree in Life Science, or a comparable degree in Computer Science, Information Technology, Clinical Information Management or equivalent. 4-6 years of experience in the pharmaceutical industry. Knowledge of and experience with AI/ML, CI/CD pipelines, Python and R. Experience with data visualisation tools such as Tableau or Power BI. A good understanding of databases and SQL. Understanding of clinical protocols, CRF standards, InForm terminology and EDC data structure. Profound knowledge of GxP and drug development guidelines. Experience in project management, collaboration and presentation. Fluent written and spoken English, cultural awareness and the ability to work in a diverse, global environment. A proactive, quality-minded approach, with strong analytical skills and the ability to plan your work. Useful, but not essential: Knowledge of clinical development and basic medical terminology. 2+ years of experience within clinical data management systems. Experience with Amazon Web Services (AWS) and REST or other APIs. Knowledge of JavaScript and the AngularJS framework.

What you’ll do

You will own your projects and work with minimal supervision, in line with Novo's SOPs and policies. Your work falls into these areas: Build, validate and deploy deep learning models for patient stratification, endpoint prediction and data anomaly detection, and manage the model lifecycle, including versioning, drift monitoring and retraining. Implement Generative AI applications, including Large Language Models (LLMs) and Retrieval-Augmented Generation (RAG) systems, to automate document processing, query clinical databases and generate insights. Build automated ETL pipelines on Azure DevOps and Databricks to harmonise complex clinical data sources. Apply DevOps and MLOps practices, CI/CD pipelines, and advanced Python and SQL to deliver reliable, scalable and secure production applications. Program, review and update complex clinical reports from documented requirements, using SQL, SAS, Python, R and CI/CD pipelines. Deliver on time, solve problems during a trial, and give stakeholders clear, actionable insight. Support leads in coordinating reporting with external partners. Design, develop and maintain dashboards and reusable visualisation components that help users understand and analyse data. Support tools for data collection, transformation and analysis, test and debug end to end, and improve older databases. Create training materials and share what you learn. Keep documentation up to date and work with subject matter experts to interpret trial operational data. Act early on concerns to protect data accuracy, consistency and completeness, and support data review training across CDMP and DSI. Lead or support small projects and give management input on improving standards and processes.

Who you’ll work with

You will be based in Data Standards and Intergration in Bangalore, India, part of Research & Development, where colleagues bring data, technology and collaboration together to move scientific ideas towards clinical testing and help meet future health needs. You will report to [insert hiring manager name and title]. Your key partners are colleagues in Clinical Operations, including Trial Project Managers and Clinical Research Associates, as well as Global IT, Global Safety and CMU. You will also work with vendors and CROs, keeping everyone informed and listening carefully when views differ. You may bring people with different interests towards new ways of working, and you will share better practice. The work is global, so cultural awareness matters. Some travel may be expected for training, collaboration and international meetings.

What you can expect here

You will be trusted to take ownership, make decisions within your area of expertise and make your voice heard. Your manager and senior colleagues are there for guidance, and you will grow through technically demanding work where innovation is part of the day-to-day, building new skills alongside colleagues across clinical operations, IT and safety. We value people who are accountable, ambitious, open and honest, and we support them to perform at their best.

Your impact begins today.

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

Experience Level Mid Level