Associate Director, Clinical Trial Procurement & Strategy

Tevapharm; Chester; Hybrid; GBP 103,000 - 148,000; Full time

Benefits offered by this job

Comprehensive Health Insurance (Health

401(k) with employer match

Paid Time Off (PTO)

Life & Disability Insurance

Employee Assistance Program

Job summary

Teva Pharmaceuticals USA seeks an Associate Director of Clinical Trial Management Business Partnering & Category Strategy to lead category management and sourcing for clinical trial services across Phases 1–4. You will partner with Clinical Development and external CROs to shape strategies for FSO, FSP, and related services, balancing cost, quality and speed.

The role is hybrid, based at our West Chester, PA site, reporting to the Director – Clinical Development Business Partnering & Category

Qualifications

• Experience in clinical development sourcing.
• Familiar with CRO and FSP/FSO models in regulated environments.
• Ability to translate study needs into practical sourcing strategies.

Responsibilities

• Partner with Clinical Development and Clinical Operations to understand study requirements and outsourcing needs.
• Develop and maintain category strategies and roadmaps for Clinical Trial Management services (FSO, FSP).
• Provide supplier insights to support decisions, supplier selection, and outsourcing model considerations.
• Lead sourcing initiatives, RFx activities, supplier evaluation, negotiations, and contracting support.
• Collaborate with Legal, Finance, Quality, Regulatory and other stakeholders to align commercial approaches.

Skills

Category management

Strategic sourcing

Supplier governance

Stakeholder management

Negotiation

Analytical thinking

Leadership

Education

Bachelor’s degree in Life Sciences / Business

Master’s degree preferred

Job description

Teva Pharmaceuticals USA seeks an Associate Director of Clinical Trial Management Business Partnering & Category Strategy to lead category management and sourcing for clinical trial services across Phases 1–4. You will partner with Clinical Development and external CROs to shape strategies for FSO, FSP, and related services, balancing cost, quality and speed.

The role is hybrid, based at our West Chester, PA site, reporting to the Director – Clinical Development Business Partnering & Category