Global Clinical Development Lead, Senior Director

Pfizer; Bothell (WA); Hybrid; USD 275,000 - 458,000; Full time

Benefits offered by this job

401(k) with Pfizer Matching

Relocation assistance

Job summary

Pfizer is seeking a Global Development Lead to serve as the single clinical accountability for development across assigned assets. You will lead a cross-functional team including clinical, pharmacology, statistics, safety, and operations to drive worldwide regulatory submissions.

You will create and endorse the Clinical Development Plan, guide protocol design, and partner with external organizations as needed.

Qualifications

• MD or DO is required.
• 8+ years in clinical development for pharma/biotech in academia and/or industry.
• Extensive knowledge of clinical development, global/regional regulation, ICH/GCP, AE management.
• Demonstrated leadership of large, cross-functional teams and strong communication skills.
• Experience designing and launching large clinical development programs, especially in obesity/internal medicine.

Responsibilities

• Lead cross-functional Clinical Development Team for assigned assets in design, execution and interpretation of studies for global submissions.
• Create and endorse Clinical Development Plan and protocol design documents.
• Drive regulatory submissions and related deliverables (SCE, SCS, overview).
• Collaborate with external partners and internal Medicine Team Leads to align milestones and budgets.
• Provide input on target product profiles, labels, Investigator Brochures, and safety reports.
• Develop development strategies including digital/innovation and patient engagement approaches.

Skills

Clinical development leadership

Cross-functional collaboration

Regulatory submission experience

Strategic planning

Trial design

Education

MD or DO

Job description

Pfizer is seeking a Global Development Lead to serve as the single clinical accountability for development across assigned assets. You will lead a cross-functional team including clinical, pharmacology, statistics, safety, and operations to drive worldwide regulatory submissions.

You will create and endorse the Clinical Development Plan, guide protocol design, and partner with external organizations as needed.