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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in advanced statistical concepts and techniques, particularly within oncology, while providing strategic leadership in clinical development projects. Proven ability to manage complex projects and ensure compliance with regulatory standards and organizational protocols.
Highest-signal resume keywords
PhD In StatisticsOncology ExperienceClinical Development ExpertiseProject Management SkillsRegulatory Submissions Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Advanced Statistical TechniquesClinical Development PlanningStatistical Analysis Plans (SAPs)Clinical Study Reports (CSRs)Regulatory Document PreparationTrial Activity ManagementOperational ExcellenceCompliance Standards
Soft Skills
LeadershipInterpersonal CommunicationCollaboration
Industry Keywords
BiotechPharmaClinical Research Organizations (CROs)Health AuthoritiesAcademic Clinical Research Centers
About the role
Key responsibilities & impact- Serve as a recognized statistical domain leader with relevant clinical knowledge in solid tumors
- Support efficient clinical development planning and study design
- Provide advanced statistical and scientific contributions to clinical development plans, protocols, SAPs, CSRs, regulatory documents, studies, and submissions
- Provide strategic statistical leadership for projects in Sanofi’s solid tumor pipeline
- Plan, monitor, and manage multiple complex projects, including trial activities, timelines, processes, and resources
- Ensure operational excellence and compliance with Sanofi SOPs and Biostatistics standards
- Collaborate with aligned project teams, statistics project leaders, and senior leadership
- Represent Statistics in regulatory meetings, scientific or technology working groups, and cross-functional initiatives
Requirements
What you’ll need- PhD in Statistics or related discipline with at least 8 years of pharmaceutical experience in clinical development, including experience with Biotech, Pharma, Clinical Research Organizations (CROs), health authorities or academic clinical research centers; OR MS in Statistics or related discipline with at least 10 years of pharmaceutical experience in clinical development, including experience with Biotech, Pharma, Clinical Research Organizations (CROs), health authorities or academic clinical research centers
- Broad knowledge and good understanding of advanced statistical concepts and techniques
- Oncology experience is required, with hands-on experience supporting clinical development programs within oncology
- Proven successful experience in clinical development, such as submissions, interactions with regulatory agencies or other external stakeholders
- Demonstrated leadership, excellent interpersonal/communication, and project management skills
- Expertise representing organizations in cross-company activities, such as consortiums or professional associations
- Experience publishing research findings, technical articles, or industry insights is preferred
Benefits
Comp & perks- People development and inclusive career opportunities
- Opportunities for growth through promotion or lateral move, at home or internationally
- Thoughtful rewards package
- Health and wellbeing benefits
- High-quality healthcare
- Prevention and wellness programs
- At least 14 weeks’ gender-neutral parental leave
- Employee benefit programs
- AI, data, and digital platforms supporting work at the forefront of drug discovery
