Job title: Early Phase Programming Team Lead

·Location: IN / Hyderabad

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. Build a career and you can be part of transforming our business while helping to change millions of lives. Ready? As an Early Phase Programming Team Lead you will Lead one or more statistical programming project team(s). Responsible for all programming activities at the project/indication level. Contribute to department initiatives and task forces

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?

Major Responsibilities:

• Programming Project Lead (PPL) of a moderate size project / one or several indications of a project in late phase clinical development or multiple projects in early or post-marketing phase. With limited direction from group manager, plan and execute statistical programming activities for responsible project(s).

• Provide leadership, guidance, and hands-on support to ensure high quality and timely statistical programming deliverables within a project, ensure technical validity, compliance to internal standards and SOPs, regulatory requirements.

• Plan and track programming project activities, timelines, and resource use in cross-site global setting; provide justification for planned resource needs, seek to optimize resource utilization thru efficient and well-managed resource allocation and across projects or areas.

• Ensure standardization and consistency in specifications and programming deliverables across individual studies and for integrated analyses. Provide technical guidance and leadership to metadata specifications and project/study specific data requirements.

• Lead regulatory submission activities, including electronic submission packages. Supervise the quality controls (QC) methods and processes for programming deliverables in both study and submission level activities.

• Provide guidance to junior staff on programming techniques, project management and implementation of standards. Collaborate effectively with project statistician and with other functions in the aligned project team; participate in clinical project meetings and provide inputs, whenever relevant

• Lead oversight activities for outsourcing engagements; guide team members to effectively interact with external resources. Participate in departmental initiatives; provide inputs to programming standardization and process optimization.

About you

• Experience: Programming experience preferably in processing clinical trial data in the pharmaceutical industry.

• Soft skills: Collaborative and progressive mindset and a potential for future, Agility to quickly acquire new skills.

• Thorough understanding of pharmaceutical clinical development (i.e., statistical concepts, techniques, and clinical trial principles) and ability to lead regulatory submissions.

• Technical skills: Excellent technical skills in statistical programming, with advanced knowledge in SAS and Knowledge about R Programming would be an advantage.

• Education: Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.

• Languages: Highly effective communication in English, both oral and written.

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.

• Build, develop and manage a statistics team support multiple TAs and different clinical phases

• Develop a career of being an influential statistician

• Gain international clinical trial experiences and communicate with Health Authorities worldwide

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!