Executive Director, Clinical Protocol Design & Delivery

Bristol Myers Squibb; Princeton (NJ); On-site; USD 298,000 - 361,000; Full time

Benefits offered by this job

Comprehensive benefits

Flexible Time Off

11 paid holidays

Job summary

Bristol Myers Squibb seeks an Executive Director to lead the Protocol Management Office (PMO) and advance clinical development quality across therapeutic areas. You will shape governance, ensure regulatory compliance, and drive strategic initiatives with senior stakeholders.

The role emphasizes leadership, cross-functional collaboration, and readiness to engage externally through industry forums while guiding training and capability-building within the CDDC.

Qualifications

• 10+ years of clinical development and execution of studies.
• Deep knowledge of regulatory/compliance requirements, clinical operations, statistics, and epidemiology.
• Experience with protocol development and review.
• Ability to lead through influence across global organizations.

Responsibilities

• Provide strategic leadership of the Protocol Management Office (PMO) and oversee review processes to ensure scientific quality.
• Lead educational and training initiatives for clinical development capabilities across the organization.
• Drive initiatives to enhance innovation, operational excellence, and efficiency in clinical development.

Skills

Leadership

Cross-functional

Regulatory awareness

Problem solving

Education

MD/PhD/PharmD/MS/RN

Job description

Bristol Myers Squibb seeks an Executive Director to lead the Protocol Management Office (PMO) and advance clinical development quality across therapeutic areas. You will shape governance, ensure regulatory compliance, and drive strategic initiatives with senior stakeholders.

The role emphasizes leadership, cross-functional collaboration, and readiness to engage externally through industry forums while guiding training and capability-building within the CDDC.