Associate Statistical Project Leader
Sanofi
June 26, 2026
Remote friendly (Morristown, NJ)
United States
$122,250 - $176,583.33 USD yearly
Clinical Research and Development
Main Responsibilities
- Lead one or several late phase studies or lead an indication for a complex compound.
- Provide high-quality input into study design, setup, and conduct; accountable for statistical aspects of the study.
- Prepare statistical methods, contribute to result interpretation, ensure statistical integrity in clinical study reports and publications; perform exploratory and ad-hoc analyses.
- Plan, monitor, and manage study activities and timelines in compliance with Sanofi SOPs and EGDS standards.
- Mentor junior project team members; promote a culture of teamwork, quality, operational efficiency, and innovation.
- Under supervision of the statistical project leader and/or team leader, oversee execution of statistical analyses and coordinate with programmers as needed.
- Develop productive collaboration with other functions in the project team.
- Represent statistics in scientific/technology working groups or cross-functional activities.
About You (Qualifications)
- PhD in statistics or related discipline with minimum 1 year of pharmaceutical clinical development experience (or MS with minimum 3 years), including experience with biotech/pharma, CROs, health authorities, and academic clinical research centers.
- Broad knowledge of advanced statistical concepts/techniques; ability to perform advanced analyses using SAS or R.
- Strong project management, interpersonal, and communication skills.
- Experience participating in cross-company and/or academia workings or special interest groups.
- Proficient in written and spoken English.
Benefits
- Health and wellbeing benefits including healthcare, prevention/wellness programs, and at least 14 weeks’ gender-neutral parental leave.
- Lead one or several late phase studies or lead an indication for a complex compound.
- Provide high-quality input into study design, setup, and conduct; accountable for statistical aspects of the study.
- Prepare statistical methods, contribute to result interpretation, ensure statistical integrity in clinical study reports and publications; perform exploratory and ad-hoc analyses.
- Plan, monitor, and manage study activities and timelines in compliance with Sanofi SOPs and EGDS standards.
- Mentor junior project team members; promote a culture of teamwork, quality, operational efficiency, and innovation.
- Under supervision of the statistical project leader and/or team leader, oversee execution of statistical analyses and coordinate with programmers as needed.
- Develop productive collaboration with other functions in the project team.
- Represent statistics in scientific/technology working groups or cross-functional activities.
About You (Qualifications)
- PhD in statistics or related discipline with minimum 1 year of pharmaceutical clinical development experience (or MS with minimum 3 years), including experience with biotech/pharma, CROs, health authorities, and academic clinical research centers.
- Broad knowledge of advanced statistical concepts/techniques; ability to perform advanced analyses using SAS or R.
- Strong project management, interpersonal, and communication skills.
- Experience participating in cross-company and/or academia workings or special interest groups.
- Proficient in written and spoken English.
Benefits
- Health and wellbeing benefits including healthcare, prevention/wellness programs, and at least 14 weeks’ gender-neutral parental leave.