Statistical Project Leader (Associate Director)
Sanofi
6 months ago
Remote friendly (Morristown, NJ)
United States
Clinical Research and Development
Main Responsibilities
- Provide a proficient level of statistical and scientific contribution to clinical development plans, studies, and submission activities (when applicable), with minimal guidance.
- Accountable for statistical aspects including quality, relevance to external stakeholders (e.g., regulatory authorities, medical journals), and scientific validity.
- Plan, monitor, and manage project activities, timelines, processes, and resources to ensure operational excellence and compliance with Sanofi SOPs and Biostatistics standards.
- Develop productive collaboration with other functions in the project team and with other statistics project leaders; communicate with senior leadership.
- Mentor junior project team members and foster productive teamwork, quality, operational efficiency, and innovation.
- Represent statistics in cross-functional and cross-company activities (e.g., working groups, consortiums, professional associations).
Qualifications
- PhD/MS in statistics or related discipline with at least 5 years of pharmaceutical experience in clinical development, including experience with biotech/pharma, CROs, health authorities, and academic clinical research centers.
- Broad knowledge of advanced statistical concepts and techniques; ability to conduct advanced analyses using SAS or R.
- Demonstrated strong project management, interpersonal, and communication skills.
- Experience representing organizations in cross-company activities (e.g., consortiums, professional associations).
- Proficient written and spoken English.
Benefits (as stated)
- Health and wellbeing benefits, including high-quality healthcare and prevention/wellness programs.
- At least 14 weeks’ gender-neutral parental leave.
- Provide a proficient level of statistical and scientific contribution to clinical development plans, studies, and submission activities (when applicable), with minimal guidance.
- Accountable for statistical aspects including quality, relevance to external stakeholders (e.g., regulatory authorities, medical journals), and scientific validity.
- Plan, monitor, and manage project activities, timelines, processes, and resources to ensure operational excellence and compliance with Sanofi SOPs and Biostatistics standards.
- Develop productive collaboration with other functions in the project team and with other statistics project leaders; communicate with senior leadership.
- Mentor junior project team members and foster productive teamwork, quality, operational efficiency, and innovation.
- Represent statistics in cross-functional and cross-company activities (e.g., working groups, consortiums, professional associations).
Qualifications
- PhD/MS in statistics or related discipline with at least 5 years of pharmaceutical experience in clinical development, including experience with biotech/pharma, CROs, health authorities, and academic clinical research centers.
- Broad knowledge of advanced statistical concepts and techniques; ability to conduct advanced analyses using SAS or R.
- Demonstrated strong project management, interpersonal, and communication skills.
- Experience representing organizations in cross-company activities (e.g., consortiums, professional associations).
- Proficient written and spoken English.
Benefits (as stated)
- Health and wellbeing benefits, including high-quality healthcare and prevention/wellness programs.
- At least 14 weeks’ gender-neutral parental leave.