Head of Trial Optimization & Feasibility

Tevapharm; West Chester (Chester County); On-site; USD 202,000 - 253,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Job summary

Teva Pharmaceuticals seeks a Senior Director, Head of Trial Optimization & Feasibility to define sponsor-side feasibility, enrollment forecasting, and protocol optimization for a global, highly outsourced clinical development portfolio. Lead analytics, set governance standards, and partner across R&D, Clinical Operations, Medical Affairs, and Vendors.

Responsibilities include building internal feasibility analytics, challenging CRO assumptions, and embedding diversity and sustainability

Qualifications

• 12+ years in global clinical development or equivalent.
• Experience leading feasibility, enrollment forecasting, and protocol optimization.
• Ability to challenge CRO enrollment assumptions in outsourced models.

Responsibilities

• Define sponsor-side feasibility standards and enrollment Forecasting.
• Lead CRO challenge sessions and governance-ready projections.
• Design and maintain sponsor-side methodology for country and site allocation.
• Drive continuous improvement of forecasting accuracy across studies and CRO partners.

Skills

Global clinical development

Feasibility leadership

CRO oversight

Forecasting analytics

Education

Bachelor's degree

Tools

Analytics tools

Job description

Teva Pharmaceuticals seeks a Senior Director, Head of Trial Optimization & Feasibility to define sponsor-side feasibility, enrollment forecasting, and protocol optimization for a global, highly outsourced clinical development portfolio. Lead analytics, set governance standards, and partner across R&D, Clinical Operations, Medical Affairs, and Vendors.

Responsibilities include building internal feasibility analytics, challenging CRO assumptions, and embedding diversity and sustainability