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Parexel

End-to-end clinical trials and regulatory consulting

Supply and Logistics Specialist

Supply Chain ManagementConfirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listedRemote

About the Job

Requirements

  • Ability to manage multiple varied tasks, prioritize workload, and maintain attention to detail.
  • Consultative selling, negotiation, communication, and customer-management skills.
  • Ability to support team members and develop creative solutions.
  • Operational understanding and basic project-management skills.
  • Proficiency with the Microsoft Office suite.
  • Good understanding of the GxP regulatory framework.
  • Extensive experience in the pharmaceutical, clinical research, or consulting industry.
  • Profound experience in clinical logistics or a related field within the biopharmaceutical industry.
  • Project-management experience and a strong understanding of cross-functional activities.
  • Profound multinational work experience.
  • Fluency in English.
  • Education to BA/BS or Master's level, or equivalent (e.g., PharmD), in biology, pharmacy, another health-related discipline, international trade, business administration, logistics, or relevant work experience.

Responsibilities

  • Engage with the SLPM to develop logistics concepts and solutions that meet client satisfaction and project profitability.
  • Monitor study scope and progress to ensure project timelines and budgets meet contractual agreements, proactively managing and communicating changes and risks.
  • Ensure study-specific management tools and documents are in place.
  • Manage assigned project resources to ensure the CTS&L FTE allocation is appropriate and meets study requirements.
  • Manage pass-through costs, including controls and reporting for internal service fees and external providers.
  • Collaborate with the team and stakeholders to develop clinical supply, sourcing, and distribution strategies and ensure required documentation is in place.
  • Communicate with third-party providers and negotiate scope of work in conjunction with procurement.
  • Develop and plan inventory based on strategy, quantities, and forecasts.
  • Develop supply schedules, seek feedback from the clinical team on study progress, adjust schedules accordingly, and provide feedback to depots.
  • Identify and initiate process improvements.
  • Mentor Clinical Supply Specialists and Clinical Supply Assistants.

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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