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Medpace

Global CRO delivering full-service clinical trials

Entry-Level Supply Chain Coordinator

Supply Chain ManagementConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in Operations, Supply Chain, or Logistics is preferred.
  • Clinical trial experience is a plus but not required.
  • Demonstrated experience working and leading in a cross-functional environment.
  • Ability to work with internal and external customers and vendors to meet project-specific goals.
  • Ability to manage high-volume work and meet rigorous deadlines.
  • Knowledge of transportation and logistics customs terminology is preferred.
  • Flexibility to strategically manage negotiations with minimal oversight.
  • Ability to interact with sites, clients, and other functional areas as the project contact for escalated supply chain issues and questions.
  • Ability to manage time and project requirements based on study deliverables.

Responsibilities

  • Continuously review open-order reports and communicate need dates to vendors.
  • Communicate delivery updates regularly with internal stakeholders and work to mitigate shortages and delays.
  • Adjust plans and iterate the supply chain setup when study requirements change.
  • Monitor the flow of goods through the inventory management system and warehouse physical storage.
  • Review study-specific inventory and alert teams to prevent stockouts.
  • Assist in maintaining and reviewing vendor performance ratings.
  • Contribute to continuous improvement initiatives that further streamline processes.

Desired Qualifications

  • Knowledge of transportation and logistics customs terminology is preferred.
  • Clinical trial experience is a plus but not required.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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