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Parexel

End-to-end clinical trials and regulatory consulting

Global Supply Sourcing Coordinator

Procurement & SourcingConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listedRemote

About the Job

Requirements

  • A bachelor's degree, master's degree, or equivalent in biology, pharmacy, another health-related discipline, international trade, business administration, or logistics, or relevant work experience.
  • An operational understanding of clinical studies, related supply chain activities, sourcing, and contracting principles.
  • Knowledge of Good Clinical Practice, Good Distribution Practice, and Good Practice requirements.
  • Strong knowledge of Microsoft Office applications.
  • Strong analytical and problem-solving skills and the ability to adapt to changing study needs.
  • Excellent interpersonal, verbal, and written communication skills.
  • The ability to prioritize work with tight timelines and significant urgency while maintaining attention to detail and first-time quality.

Responsibilities

  • Maintain close working relationships with internal and external customers and provide professional sourcing advice and assistance at all levels.
  • Monitor quality, pricing accuracy, purchase requests, approvals, and purchase orders.
  • Conduct commodity research, regulatory requirements research, supplier selection, and requests for information, quotations, and proposals.
  • Ensure products and services are obtained at budgeted prices and that ancillary materials and investigational products meet local requirements.
  • Coordinate the return of rental equipment and medical devices.
  • Own and action sourcing help desk tickets, create and execute Statements of Work, and complete on-demand sourcing activities that support study needs.
  • Anticipate sourcing challenges, take ownership through resolution, and work with suppliers to identify comparable compliant ancillary supplies.
  • Obtain required supplier and manufacturer documentation for import and export activities.
  • Take action on quality issues involving third-party suppliers and manage risk mitigation through resolution.
  • Assist internal customers with sourcing questions and system challenges and mentor junior team members.

Desired Qualifications

  • Four or more years of sourcing or procurement experience in a contract research organization or pharmaceutical environment.
  • Knowledge of sourcing operations and supplier management.
  • Cross-functional business team experience.
  • Process and project management capabilities.

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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