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Parexel

End-to-end clinical trials and regulatory consulting

Vendor Strategy Director

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listedRemote

About the Job

Requirements

  • Strengths in strategic thinking, business partnership, relationship building, and influencing across complex matrix organizations.
  • Experience leading vendor strategy, outsourced clinical trial activities, and cross-functional clinical operations initiatives.
  • Ability to build and maintain effective external partnerships and internal stakeholder relationships.
  • Strong understanding of clinical development, clinical trial operations, and supplier management principles.
  • Excellent communication, planning, project management, analytical, and problem-solving capabilities.
  • Ability to navigate complex environments while balancing quality, timelines, innovation, and business priorities.
  • Advanced degree in science or business, or equivalent relevant experience.
  • 10+ years of relevant industry experience, including leadership within clinical operations and management of outsourced clinical trial activities at both operational and strategic levels.
  • Strong understanding of clinical trial methodology, Good Clinical Practice (GCP), medical terminology, and clinical development processes.
  • Experience with supplier services supporting clinical development programs and a strong understanding of trial management and trial monitoring activities.
  • Knowledge of quality and regulatory standards relevant to clinical research and outsourced service delivery.
  • Demonstrated success developing and managing strategic internal and external partnerships.
  • Strong communication, organizational, leadership, and problem-solving skills.
  • Fluent written and spoken English.

Responsibilities

  • Lead end-to-end supplier and vendor strategy activities across clinical development programs.
  • Define and align program-level vendor strategies in partnership with Clinical Operational Program Heads, Portfolio Innovation Directors, Procurement, and alliance stakeholders.
  • Manage and oversee supplier performance against established program objectives and strategic priorities.
  • Proactively identify, assess, and manage supplier risks, quality concerns, and contract-related issues while driving continuous improvement initiatives.
  • Anticipate future portfolio and program needs and translate upcoming demand into vendor service requirements.
  • Partner with vendor alliance teams to identify, qualify, and engage suppliers that support evolving program needs.
  • Enable early supplier engagement during protocol development and feasibility activities to support operational readiness.
  • Serve as the primary point of contact and escalation for program-level vendor strategy and operational challenges.
  • Drive productivity initiatives and oversee achievement of vendor-related performance objectives.
  • Support inspection readiness and audit-related activities across programs.
  • Provide operational and functional support to Trial Vendor Managers and Vendor Start-up Managers.
  • Collaborate with global stakeholders to leverage innovative vendor solutions that enhance clinical trial execution and delivery.

Desired Qualifications

  • Experience partnering with global, cross-functional clinical development organizations.
  • Demonstrated executive leadership and strategic vendor management experience.
  • Experience driving productivity initiatives and operational improvements across clinical programs.
  • Experience supporting inspection readiness, audit preparation, and quality-focused supplier management.
  • Track record of enabling successful international collaboration across diverse stakeholder groups.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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