Principal Data Management Programmer

Sanofi; Hyderabad; On-site; INR 800,000 - 1,500,000; Full time

Benefits offered by this job

High-quality healthcare

Wellness programs

Parental leave

Career development opportunities

Supportive team environment

Job summary

Join a forward-thinking global healthcare company as a Principal Data Management Programmer in Hyderabad. In this pivotal role, you will lead the development of data validation programs and analytics, supporting clinical studies that impact millions of lives. Collaborate with a diverse team to innovate and optimize data management processes while enhancing your career in a supportive environment. This position offers the chance to work on groundbreaking projects, implement advanced data solutions, and contribute to the evolution of Clinical Data Management. If you're ready to make a difference and grow your expertise in a dynamic setting, this opportunity is perfect for you.

Qualifications

• Strong programming experience in SAS, R, or Python with data visualization tools.
• Advanced project management and communication skills are essential.

Responsibilities

• Develop data validation programs and analytics for clinical projects.
• Manage technical writing and optimize reporting tools.

Skills

SAS Programming

R/R Shiny

Python

Data Visualization Tools

Project Management

Communication Skills

Intercultural Skills

Education

Bachelor of Science

Master of Science

Tools

Power BI

Spotfire

Tableau

SAS

Job description

Job title: Principal Data Management Programmer

• Location: Hyderabad, India

About the job

Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Join our Hyderabad Hub, build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As Principal Data Management Programmer within our Hyderabad Hub, you’ll be responsible for developing programs for data validation, data review, and protocol deviation deliverables for assigned projects, providing timely support to Study Team(s) on data management programming or data visualization analytics according to project data cleaning strategies through project milestones from study start-up to database lock.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

• Developing listings, summary tables, figures and/or advanced analytics for data validation, data review, medical review, AE dedicated review, and SAE reconciliation.

• Distributing and/or deploying data review and data validation solutions which check all collected data including external data (i.e., cross-panel checks and internal/external data reconciliation).

• Developing automatic protocol deviations identification solutions.

• Liaising with standard Data Reporting Analyst (DRA) to continuously maintain and optimize the existing standard reporting tools, programs, and report library.

• Developing efficient Power BI, Spotfire, R/Shiny & SAS standard packages facilitating the programming of study solutions.

• Managing the technical writing at CTT level (i.e., user guides, detailed specifications, best practices, programming conventions, etc.).

• Analyzing new requirements from customers and proposing technical solution strategies.

About you

• Experience: Strong SAS programming experience or equivalent programming language experience such as R/R shiny, Python, or equivalent data visualization tools experience such as Spotfire, Power BI, Tableau. In addition, clinical trial experience, clinical data management experience, and pharmaceutical industry experience are preferred.

• Soft and technical skills: Advanced project management skills.

• Advanced collaboration and communication skills.

• Outstanding capability of independent thinking and delivery of accurate outcomes. Meeting management skills such as organizing meetings and discussions. Crystal clear logical thinking. Good coaching and people development skills. Intercultural skills with the ability to work effectively in a multi-cultural context.

• Expertise in programming languages such as SAS, R, and Python.

• Expertise in database structure and data flow. Knowledge of industry standards and practices (e.g., CDISC especially CDASH and SDTM). Knowledge of data visualization tools such as Spotfire, Power BI, Tableau.

• Experience in implementing and fine-tuning AI/ML models.

• Strong knowledge of current regulatory guidelines and GCP practices regarding Data Management.

• Understanding of advanced drug development concepts such as Decentralized Clinical Trials (DCT), Master & Adaptive Protocols, eSource, and AI-Based automations is a plus.

• Education: Bachelor or Master of Science degree or above, preferably in a life science or mathematics-related area (e.g., Pharmaceutical, medical, or mathematics, computer science or similar technical fields).

• Languages: Strong English skills (verbal and written), ability to exchange fluently in a global environment.

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team.

• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender-neutral parental leave.

• Join an international innovative biopharma company.

• Lead data management programming activities and serve as an expert working on several therapeutic areas.

• Participate in the evolution of Clinical Data Management and deployment of innovations.

“As a principal data management programmer in our India Hub, you’ll get the opportunity to lead data management programming for global studies in different therapeutic areas and act as the expert to develop your career in the global organization. Join the Best, Be the Best!”