Associate Director - Clinical Sciences

Teva Pharmaceutical Industries Ltd. West Chester, US Posted Aug 12, 2026
Location
West Chester, US
Workplace
On-site / per employer
Posted
Aug 12, 2026

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration.

You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

The Associate Director – Clinical Sciences Business Partnering & Category Strategy is an experienced procurement professional responsible for category management and sourcing for Clinical Sciences services. The role translates laboratory, biomarker, sample, and study needs into sourcing and supplier strategies that support cost, quality, speed, data integrity, and business objectives.

Reporting to the Director – Clinical Development Business Partnering & Category Strategy, this role is responsible for assigned categories including global central labs, specialty and biomarker laboratories, Translational & Precision Medicine, and biorepository services. The Associate Director develops category plans, leads sourcing initiatives, supports supplier performance, and provides market and commercial insights within this defined scope.

The successful candidate combines clinical laboratory knowledge, commercial judgment, analytical capability, strong stakeholder partnership, and a hands-on approach.

This role is hybrid 2-3 days in our West Chester, PA site.

How You’ll Spend Your Day

Business Partnering & Category Strategy

  • Partner with Clinical Development, Translational & Precision Medicine, Clinical Operations, and other stakeholders to understand laboratory, biomarker, sample, study, and business requirements.
  • Develop and maintain category strategies and sourcing roadmaps for central labs, specialty and biomarker laboratories, Translational & Precision Medicine, and biorepository services.
  • Provide category and supplier insights to support business decisions, supplier selection, and service-model considerations.

Category Analytics, Productivity & Value Creation

  • Use spend data, testing volumes, supplier insights, benchmarks, and market intelligence to identify sourcing, productivity, and value opportunities.
  • Develop category-level value initiatives such as pricing optimization, preferred-provider adoption, demand management, supplier consolidation, testing standardization, and logistics optimization.
  • Track sourcing outcomes, value delivery, and key category activities using established Procurement tools and reporting mechanisms.

Strategic Supplier Management & Market Intelligence

  • Support supplier segmentation, governance, performance management, and improvement activities for key Clinical Sciences suppliers.
  • Maintain current knowledge of supplier capabilities, service models, capacity, pricing dynamics, technology trends, and relevant regulatory or quality considerations.
  • Use supplier and market insights to improve sourcing decisions and support supplier performance, continuity, sample integrity, and data quality.

Strategic Sourcing & Commercial Enablement

  • Lead or support sourcing initiatives for Clinical Sciences services, including requirements, RFx activities, supplier evaluation, negotiation, recommendation, and contracting support.
  • Partner with Strategic Sourcing, Legal, Finance, Quality, Regulatory, Clinical Development, and scientific stakeholders on commercial approaches and supplier agreements.
  • Balance cost, quality, speed, scientific capability, data and sample integrity, compliance, continuity, and supplier capability in sourcing recommendations.

Procurement Process & Capability Support

  • Apply established category management, sourcing, supplier governance, and value-tracking practices across assigned work.
  • Contribute insights and lessons learned that improve Procurement tools, processes, supplier governance, and stakeholder engagement.
  • Provide project leadership and subject-matter guidance to cross-functional teams and sourcing partners without direct people-management accountability.

Your Skills and Experience

  • 7+ years of progressive experience in procurement, category management, strategic sourcing, supplier management, clinical sciences, laboratory services, clinical operations, or related disciplines in life sciences or regulated environments.
  • Experience supporting sourcing, category management, supplier governance, or commercial activities for clinical laboratory, biomarker, Translational & Precision Medicine, biorepository, or related services.
  • Working understanding of drug development, clinical laboratory operations, biomarker and sample lifecycle requirements, supplier ecosystems, and relevant quality and regulatory requirements.
  • Demonstrated ability to manage cross-functional sourcing projects, analyze commercial information, influence stakeholders, and deliver measurable outcomes within an assigned scope.

LEADERSHIP COMPETENCIES & SKILLS

  • Experienced category and sourcing professional who translates scientific and business requirements and market insights into practical procurement actions.
  • Effective business partner who communicates clearly, builds credibility, and influences stakeholders within assigned categories and projects.
  • Strong commercial, analytical, organizational, and project leadership skills with a hands-on, execution-oriented approach.

EDUCATION & EXPERIENCE

  • Bachelor’s degree required; advanced degree preferred in Business, Supply Chain, Life Sciences, Finance, or related field.
  • Master’s degree with 5+ years of relevant experience, or Bachelor’s degree with 7+ years of relevant experience.
  • Prior experience leading complex projects or cross-functional teams preferred; direct people-management experience is not required.

Also Good to Have

  • Experience supporting Clinical Sciences sourcing, including central labs, specialty or biomarker laboratories, Translational & Precision Medicine, biospecimen logistics, biorepository, or related laboratory services.
  • Experience with preferred provider programs, supplier governance, test or assay pricing, sample logistics and storage, commercial negotiations, and laboratory or scientific services agreements.

Salary Range

How We’ll Take Care of You

We offer a competitive benefits package, including

  • Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
  • Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
  • Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
  • Life and Disability Protection: Company paid Life and Disability insurance.
  • Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.

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Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to AskHR@tevapharm.com with the nature of your request and your contact information.

Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.

Important notice to Employment Agencies - Please Read Carefully

Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place.

Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Originally posted by Teva Pharmaceutical Industries Ltd.. View original posting

Associate Director - Clinical Sciences at Teva Pharmaceutical Industries Ltd. | BioCareerAI