Global Trial Optimization & Feasibility Lead

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

Benefits offered by this job

Health Insurance

401(k) with company match

Paid time off

Life & Disability Insurance

Bonus potential

Job summary

Teva Pharmaceuticals is seeking a Senior Director, Head of Trial Optimization & Feasibility to govern sponsor-side feasibility, enrollment forecasting, and protocol optimization across a global development portfolio.

You will lead analytics and modeling, ensure evidence-based strategies, and collaborate across R&D, Medical Affairs, and CRO partners to drive portfolio performance and risk mitigation.

Qualifications

• 12+ years of global clinical development experience with trial optimization and feasibility leadership.
• Proven ability to challenge CRO enrollment assumptions in outsourced models.
• Bachelor’s Degree required.

Responsibilities

• Define sponsor-side feasibility standards and assess CRO packages.
• Develop enrollment forecasts using epidemiology and portfolio data.
• Endorse country/site strategies before execution.
• Lead protocol operability reviews to reduce startup risk.
• Drive continuous improvement and forecast accuracy across studies.

Skills

Trial optimization

Feasibility leadership

Global clinical development

Enrollment forecasting

Stakeholder alignment

Education

Bachelor’s degree

Job description

Teva Pharmaceuticals is seeking a Senior Director, Head of Trial Optimization & Feasibility to govern sponsor-side feasibility, enrollment forecasting, and protocol optimization across a global development portfolio.

You will lead analytics and modeling, ensure evidence-based strategies, and collaborate across R&D, Medical Affairs, and CRO partners to drive portfolio performance and risk mitigation.