Join Sanofi as a Global Study Data Leader and play a pivotal role in accelerating drug discovery and development. You'll oversee data management activities for clinical trials, ensuring compliance with regulatory standards while collaborating with cross-functional teams. Your expertise will be essential in driving efficiency and quality in our data processes.
Key Responsibilities
Lead end-to-end data management activities for clinical trials
Coordinate cross-functional teams to ensure trial compliance
Oversee vendor activities and identify risks
Ensure data quality and integration activities
Develop retro planning for key deliverables
Drive inspection readiness for data management documents
Required Qualifications
Bachelor’s degree or above in a life science or health-related field
5+ years of experience in Clinical Data Management
2+ years of project management experience in Data Management
Clinical Data Management System experience (CDMS)
Understanding of industry standards and regulatory guidelines
Preferred Qualifications
Experience with CDISC SDTM and MedDRA
Ability to present data management topics at a conference
Benefits & Perks
High-quality healthcareWellness programsAt least 14 weeks of gender-neutral parental leaveOpportunities for career growth