Director R&D Procurement - Clinical Trial Management

Teva; West Chester (Chester County); Presencial; USD 180.000 - 250.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

401(k) retirement plan

Paid time off

Descripción de la vacante

Teva Pharmaceuticals is seeking a Director of R&D Procurement – Clinical Trial Management to lead category strategy and supplier partnerships across global CROs and FSOs. The role partners with clinical development to translate study needs into sourcing strategies that drive value and resilience.

The successful candidate will shape category roadmaps, mentor sourcing professionals, and drive continuous improvement while balancing cost, quality, and regulatory requirements.

Formación

• 10+ years of progressive experience in procurement, category management, strategic sourcing, or related disciplines.
• Experience supporting clinical supply, R&D, life sciences, or regulated environments.
• Ability to influence senior stakeholders and translate priorities into procurement strategies.
• Strong commercial, analytical, and strategic capabilities.

Responsabilidades

• Partner with Clinical Development and R&D leaders to align procurement strategies with business priorities.
• Lead category strategy development and multi-year roadmaps across clinical trial management.
• Develop category productivity roadmaps to optimize cost and supplier performance.
• Maintain market intelligence and supplier insights to inform decisions.
• Provide leadership to category managers and drive capability growth.
• Balance cost, quality, speed, and compliance in sourcing strategies.

Conocimientos

Strategic procurement

Category management

Supplier relationship management

Stakeholder influence

Analytical skills

People leadership

R&D procurement

Educación

Bachelor’s degree in Business, Supply Chain, Life Sciences, Finance, or related field

Master’s degree (preferred) with 8+ years of relevant experience

Descripción del empleo

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 Director R&D Procurement – Clinical Trial Management is a strategic procurement leader responsible for leading and advancing category management across Teva’s global Clinical Trial Management organization across Phases 1-4. The role partners with clinical development and other stakeholders to translate study needs, outsourcing requirements, market intelligence, and supplier capabilities into sourcing and supplier strategies that drive value, improve supplier performance, strengthen resilience, and support business objectives.

Reporting to the Sr. Director Global Procurement – Research & Development, this leader provides strategic direction to category managers and sourcing professionals across Clinical Trial Management categories, with primary focus on Full-Service Outsourcing (FSO), Functional Service Providers (FSP), and related clinical operations services. The role is accountable for developing category strategies, strengthening strategic supplier partnerships, building productivity roadmaps, improving supplier resilience and business continuity, and advancing Procurement’s role as a trusted business partner.

The successful candidate is a strategic procurement leader who can operate across a complex global pharmaceutical environment, balancing category strategy, stakeholder influence, supplier partnership development, team leadership, and continuous improvement to further mature Procurement as a trusted value-creation partner.

How You’ll Spend Your Day

Business Partnering & Category Strategy

• Partner with Clinical Development and R&D leaders to align procurement strategies with business priorities, portfolio needs, and long-term objectives.
• Lead category strategy development, prioritization, and multi-year roadmaps across clinical trial management categories, translating business needs, spend insights, market intelligence, and supplier capabilities into actionable strategies.
• Serve as the Procurement category expert, providing strategic insights and recommendations to influence business decisions.

Category Analytics, Productivity & Value Creation

• Develop category productivity roadmaps that identify opportunities to optimize cost, improve supplier performance, reduce risk, and create measurable business value.
• Leverage spend analytics, supplier insights, benchmarking, and market intelligence to identify opportunities and guide strategic decisions.
• Establish value plans, performance measures, and reporting mechanisms to demonstrate category impact and outcomes.

Strategic Supplier Management & Market Intelligence

• Develop strategic supplier relationship strategies for critical clinical development suppliers, including supplier segmentation, governance models, performance expectations, and executive engagement.
• Maintain external market intelligence and supplier capability perspectives across CROs, FSP/FSO models, and clinical operations suppliers to inform category strategies and business decisions.
• Leverage supplier insights to identify innovation opportunities, strengthen partnerships, and improve business outcomes.

Procurement Leadership & Capability Development

• Provide leadership, coaching, and strategic direction to category managers and sourcing professionals, establishing priorities, accountability, and capability growth.
• Build scalable category management practices, governance models, and ways of working that strengthen Procurement effectiveness and stakeholder engagement.
• Drive change and continuous improvement to advance Procurement’s role as a strategic business partner.

Strategic Sourcing & Commercial Enablement

• Ensure category strategies translate into effective sourcing approaches, supplier strategies, and commercial outcomes in partnership with sourcing, Legal, Finance, Quality, Regulatory, and business stakeholders.
• Balance cost, quality, speed, flexibility, innovation, compliance, supplier sustainability, and resilience when developing procurement strategies and recommendations.

Your Skills and Experience

PROFESSIONAL EXPERIENCE & EXPERTISE

• 10+ years of progressive experience in procurement, category management, strategic sourcing, supplier relationship management, or related disciplines, with significant experience supporting clinical supply, R&D, life sciences, pharmaceuticals, biotechnology, or other regulated environments.
• Demonstrated success developing category strategies, supplier strategies, productivity initiatives, and business partnerships within complex global organizations.
• Strong understanding of pharmaceutical drug development, clinical development operating models, outsourcing strategies, supplier ecosystems, and regulatory requirements.
• Proven ability to influence senior stakeholders, translate business priorities into procurement strategies, and deliver measurable business value through strong commercial, analytical, and strategic capabilities.

LEADERSHIP COMPETENCIES & SKILLS

• Strategic procurement leader who connects business priorities, supplier ecosystems, and market intelligence to create value.
• Trusted business partner who influences stakeholders, challenges constructively, and enables effective decision-making.
• Strong category, commercial, analytical, and people leadership capabilities with the ability to drive change, build capability, and deliver outcomes through others.

EDUCATION & EXPERIENCE

• Bachelor’s degree required; advanced degree preferred in Business, Supply Chain, Life Sciences, Finance, or related field.
• Master’s degree with 8+ years of relevant experience, or Bachelor’s degree with 10+ years of relevant experience.
• Minimum five years of direct people leadership, team leadership, and/or significant matrix leadership experience.

Also Good to Have

PREFERRED / DIFFERENTIATING EXPERIENCE

• Experience supporting Phase 1-4 clinical trial management sourcing, including CRO, FSO, FSP, monitoring study management, site management, or related clinical operations services.
• Experience building category management capabilities, strategic supplier relationship programs, supplier governance models, or procurement operating models.
• Experience supporting global R&D organizations within complex pharmaceutical environments and leveraging procurement technologies, analytics, or digital capabilities.

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.

The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

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 [e-mail] 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.