Statistical Project Leader (Associate Director)
Sanofi
6 months ago
Remote friendly (Cambridge, MA)
United States
Clinical Research and Development
Main Responsibilities:
- Proficient level of statistical and scientific contribution to clinical development plans, studies and submission activities (when applicable), with minimal guidance from senior statistical project leader or team leader
- 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 aligned project team and with other statistics project leaders; communicate with senior leadership
- Mentor junior project team members and foster a culture of 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, Clinical Research Organizations (CROs), health authorities, and academic clinical research centers
- Broad knowledge of advanced statistical concepts and techniques; ability to perform advanced statistical 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 in written and spoken English
Benefits:
- Health and wellbeing benefits including high-quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender-neutral parental leave
- Proficient level of statistical and scientific contribution to clinical development plans, studies and submission activities (when applicable), with minimal guidance from senior statistical project leader or team leader
- 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 aligned project team and with other statistics project leaders; communicate with senior leadership
- Mentor junior project team members and foster a culture of 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, Clinical Research Organizations (CROs), health authorities, and academic clinical research centers
- Broad knowledge of advanced statistical concepts and techniques; ability to perform advanced statistical 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 in written and spoken English
Benefits:
- Health and wellbeing benefits including high-quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender-neutral parental leave