Associate Director, Clinical Program Sourcing & Contracting
Biogen
This listing was originally posted on Biogen's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moAbout This Role
We are building a high-performing clinical contracting capability that accelerates clinical trial delivery while strengthening compliance, financial discipline, and inspection readiness. You will lead a team of procurement associates in the Clinical Program Sourcing & Contracting (CPSC) ensuring end-to-end execution across demand planning, sourcing and contracting activities supporting global clinical programs (e.g., Phase I–IV).
This role is accountable for operational excellence, contractual compliance, and delivery performance across CPSC remit. You will collaborate closely with Clinical Services Category Management, Clinical Trial Development Unit (CTDU), and Strategic Resourcing & Performance Optimization (SRPO) teams to align study contracting timelines, specifications collection, budget validation, and contract execution.
You will also establish and lead a robust Vendor Demand Management Model across TAs, programs, and studies, ensuring consistent translation of program-level outsourcing strategies into study-level execution. The focus is to create a lean, predictable model that improves speed, quality, and stakeholder confidence. This role reports into the Head of Research, Development & Medical Services within the Global Procurement organization.
What You’ll Do
Operational Excellence – Demand planning and Clinical Contract Delivery
Lead end-to-end Demand planning and Clinical Contract Delivery operations supporting global clinical trials (Phase I–IV), ensuring timely, compliant execution of sourcing and contracting activities.
Design and optimize a scalable CPSC operating model aligned to portfolio growth.
Establish a technology-enabled Demand planning and Clinical contract delivery environment. Implement predictive contracting capabilities using historical study data and demand trends.
Define and monitor KPIs (cycle time, quality, compliance, stakeholder satisfaction) and deliver performance transparency to senior leadership.
Lead continuous improvement initiatives across SOPs, templates, legal support models, training, and systems.
Demand & Planning – Program-Level Alignment & Resource Optimization
Establish and oversee an integrated Vendor Demand Management Model ensuring consistent program-level outsourcing strategies are implemented effectively at study level.
Translate program and portfolio forecasts into structured resource capacity planning and prioritization frameworks.
Ensure clear handoffs of study specifications and contracting requirements into CPSC execution teams.
Serve as escalation point for contracting risks, timeline conflicts, and cross-functional barriers impacting study start-ups.
Commercial Governance – Financial Discipline & Contractual Controls
Drive financial transparency and discipline across contracting activities, including Fair Market Value (FMV) governance, milestone-payment alignment, and value reporting.
Develop and report Commercial Framework Contractual Compliance Metrics, tracking adherence to approved rate cards, templates, commercial protections, and negotiated terms.
Ensure audit readiness, regulatory compliance, and strong documentation practices.
Monitor contractual control effectiveness, identifying systemic gaps and leading corrective process enhancements.
Supplier Excellence – Risk Management & Performance Enablement
Implement an integrated supplier risk and performance management framework.
Establish standardized mechanisms to monitor vendor performance indicators (budget accuracy, scope stability, cycle-time adherence, inspection findings).
Who You Are
10+ years of experience in contracting, ideally within biotech/pharma and clinical trial operations.
Previous experience managing teams, setting departmental priorities to support business objectives, matrixed environment
Strong understanding of clinical trial operations and the drivers of contracting speed.
Deep knowledge of end-to-end Source to Contract processes, complex negotiations, and contract lifecycle management in a regulated environment.
Highly effective stakeholder partner with the ability to persuade and build strong relationships across technical and operational teams.
Data-driven and performance-oriented; experienced in establishing KPIs, dashboards, and reporting to drive transparency and continuous improvement.
Excellent communication and presentation skills, with the ability to communicate clearly with leaders and technical stakeholders
Process-oriented, continuous improvement mindset; Identifies and solves complex, operational and organizational problems
Education:
Bachelor’s degree required; advanced degree and/or legal/contracting background is a plus; relevant certifications (e.g., CPSM/C.P.M.) are desirable.
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Additional Information
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
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