Associate Director, Biostatistics — Drug Development Leader

Bristol Myers Squibb; Princeton (NJ); Presencial; USD 190.000 - 230.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Time Off

11 paid holidays

Wellbeing programs

Descripción de la vacante

Bristol Myers Squibb in Princeton, NJ is seeking an Associate Director of Biostatistics to lead cross-functional trial design and analyses for regulatory submissions. The role involves designing innovative trials, authoring key statistical documents, and providing strategic statistical support across multiple studies.

The candidate should have a PhD or MS with extensive experience in statistics/biostatistics, proficiency in SAS/R/Python, and strong communication skills to collaborate with

Formación

• PhD (6+ years) or MS (8+ years) in statistics/biostatistics with clinical trials experience.
• Proficiency in SAS, R or Python and advanced statistical methods.
• Excellent written and spoken communication and strong organizational skills.
• Expertise in statistical/clinical trials methodology for clinical development.
• Good understanding of regulatory landscape and regulatory interactions.
• Demonstrate collaboration, leadership and ability to manage multiple work streams.

Responsabilidades

• Design innovative and efficient clinical trials and select study endpoints.
• Defend protocols and analysis plans in governance reviews and provide reviews of complex protocols.
• Author/review protocols, SAPs, CSRs, and related study documents.
• Present data summaries and analyses clearly and completely.
• Provide statistical support for health authority requests, publications, and disclosures.
• Lead multiple studies to ensure consistency and adherence to standards.

Conocimientos

Interpersonal skills

Communication

Leadership

Regulatory understanding

Educación

PhD

MS

Herramientas

SAS

R

Python

Descripción del empleo

Bristol Myers Squibb in Princeton, NJ is seeking an Associate Director of Biostatistics to lead cross-functional trial design and analyses for regulatory submissions. The role involves designing innovative trials, authoring key statistical documents, and providing strategic statistical support across multiple studies.

The candidate should have a PhD or MS with extensive experience in statistics/biostatistics, proficiency in SAS/R/Python, and strong communication skills to collaborate with