Deputy Director - Senior Project Biostatistics Lead- Vaccines
Sanofi
June 30, 2026
Remote friendly (Swiftwater, PA)
United States
$148,500 - $214,500 USD yearly
Clinical Research and Development
Deputy Director - Senior Project Biostatistics Lead (Vaccines)
Main Responsibilities:
- Develop end-to-end clinical development plans with clinical/medical and global project teams; support internal approvals.
- Gain Health Authorities acceptance of statistical plans (seek input from Biostat Franchise Lead as needed).
- Oversee clinical trial execution: data capture, randomization, Statistical Analysis Plans, and analyses for primary and secondary objectives.
- Lead the most complex/priority studies; mentor team members; drive teamwork, quality, operational efficiency, and innovation; ensure compliance with SOPs and departmental standards.
- Communicate trial results internally; collaborate cross-functionally on scientific interpretation and strategic impact; contribute to Health Authorities communications.
- Be accountable for statistical aspects of submissions for marketing authorization or label improvement.
About You (Qualifications):
- PhD/MS in Statistics/Biostatistics or related discipline with at least 6 years of pharmaceutical experience.
- Proven experience in clinical development or post-marketing activities (e.g., submissions, regulatory or external stakeholder interactions).
- Broad knowledge of advanced statistical concepts and techniques.
- Strong study management, interpersonal, and communication skills.
Benefits (as stated):
- Health and wellbeing benefits including high-quality healthcare and prevention/wellness programs; at least 14 weeks’ gender-neutral parental leave.
Main Responsibilities:
- Develop end-to-end clinical development plans with clinical/medical and global project teams; support internal approvals.
- Gain Health Authorities acceptance of statistical plans (seek input from Biostat Franchise Lead as needed).
- Oversee clinical trial execution: data capture, randomization, Statistical Analysis Plans, and analyses for primary and secondary objectives.
- Lead the most complex/priority studies; mentor team members; drive teamwork, quality, operational efficiency, and innovation; ensure compliance with SOPs and departmental standards.
- Communicate trial results internally; collaborate cross-functionally on scientific interpretation and strategic impact; contribute to Health Authorities communications.
- Be accountable for statistical aspects of submissions for marketing authorization or label improvement.
About You (Qualifications):
- PhD/MS in Statistics/Biostatistics or related discipline with at least 6 years of pharmaceutical experience.
- Proven experience in clinical development or post-marketing activities (e.g., submissions, regulatory or external stakeholder interactions).
- Broad knowledge of advanced statistical concepts and techniques.
- Strong study management, interpersonal, and communication skills.
Benefits (as stated):
- Health and wellbeing benefits including high-quality healthcare and prevention/wellness programs; at least 14 weeks’ gender-neutral parental leave.