Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
SG
Sanofi Group
Project Programming Lead
Job Description
Sanofi Careers
English
Sign In
Search for Jobs
Project Programming Lead page is loaded
Project Programming Lead
Apply
locations
Morristown, NJ
Waltham, MA
Swiftwater, PA
time type
Full time
posted on
Posted 4 Days Ago
time left to apply
End Date:
September 25, 2026 (23 days left to apply) job requisition idR2864855
Job title:Project Programming Lead Location:
Morristown, NJ About the Job As Project Programming Lead within our Vaccines Biostatistical Sciences team, you'll lead the scientific programming of a large or couple of small project(s) from our vaccines portfolio, bringing data to life along the development value chain. Assume responsibility for all scientific programming activities related to a late phase clinical development project or multiple projects in early or post-marketing phase. The incumbent provides technical and operational leadership, accountable for all programming activities for the related project(s). In addition, assume transversal responsibility like outsourcing operation management. Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R D, you'll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi We're an R D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system- and innovative pipeline
- enables us to invent medicines and vaccines that treat and protect millions of people around the world.
- Provide leadership, guidance and hands-on support to ensure high-quality, timely programming outputs while ensuring compliance with internal standards, SOPs and regulatory requirements. Manage project planning & resources
- Plan and track programming activities, timelines, and resource utilization in a global setting. Ensure standardization & consistency
- Maintain consistency in specifications and programming deliverables across individual studies and integrated analyses. Drive regulatory submissions
- Lead regulatory submission activities, including electronic submission packages, ensuring CDISC data packages comply with Health Authority expectations (FDA, PMDA, CDE, KFDA, etc.). Oversight activities for outsourcing engagements and guide team interactions with external resources. Collaborate cross-functionally
- Partner effectively with project statistician(s); participate in clinical project meetings and contribute relevant inputs.
- Provide guidance to junior staff on programming techniques and standards implementation.
- people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
- $176.