Global Clinical Development Lead, Internal Medicine

Pfizer; Elkview (WV); Hybrid; USD 215,000 - 358,000; Full time

Benefits offered by this job

Relocation assistance

Hybrid/On-site work schedule

Job summary

Pfizer is seeking a Global Development Lead to represent Clinical on the Global Medicine Team, serving as the single clinical accountability for development of assigned assets in Internal Medicine. You will lead a cross-functional team across clinical, pharmacology, statistics, safety, and operations for worldwide regulatory submissions.

You will oversee the Clinical Development Plan, protocol design, and interaction with external partners.

Qualifications

• Experience leading cardiometabolic late-stage development programs.
• Knowledge of clinical development, regulatory requirements (ICH/GCP) and global submissions.
• Ability to manage large, cross-functional teams and communicate across stakeholders.

Responsibilities

• Partner with Prod Team Lead to align milestones, budget, and timelines for the clinical program.
• Develop comprehensive clinical development plan to secure global approval and reimbursement, including pediatric studies.
• Provide input for target product profile and regulatory activities (labels, CSRs, XML materials).
• Lead regulatory submissions and contribute to submission deliverables (SCE, SCS, clinical overview).
• Support trial design, monitoring, and data interpretation for multiple studies.
• Ensure compliance with SOPs and regulatory standards in all activities.

Skills

Leadership

Clinical development

Cross-functional leadership

Regulatory submissions

Trial design

Education

Bachelor's degree (BS) or PhD

Job description

Pfizer is seeking a Global Development Lead to represent Clinical on the Global Medicine Team, serving as the single clinical accountability for development of assigned assets in Internal Medicine. You will lead a cross-functional team across clinical, pharmacology, statistics, safety, and operations for worldwide regulatory submissions.

You will oversee the Clinical Development Plan, protocol design, and interaction with external partners.