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Salary
≈ $33k – $48k per year (Estimated)
Location
In office (Manchester)
Visa
Licensed UK visa sponsor
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 25, 2026. First seen by Alion on Oct 20, 2026. IQVIA scores B on the Alion truth index.

Overview
Company
Impact
Profile match
IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

Internal Job Description

Job Overview

The Clinical Supply Coordinator ensures the on-time delivery of supplies (Investigational Medicinal Products and Non-Investigational Medicinal Products) to clinical sites for established clinical trials contracted to IQVIA. This is achieved through effective inventory monitoring, ongoing forecasting of drug demand, initiation and delivery of packaging campaigns and a strong distribution strategy.

Essential Functions

  • Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time
  • Maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements
  • Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery
  • Monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed
  • Responsible for the distribution plan and has oversight of the assigned vendor(s) executing it
  • Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations
  • Maintains 100% compliance on all assigned training and applies learnings to everyday practice
  • Remain up to date in all GxP and regulatory requirements applicable to the role
  • Leads client and vendor related meetings where necessary to discuss Clinical Supply Chain topics or status updates
  • Provides administration support to the Clinical Trial Supplies team where required
  • Manages the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team
  • Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed Qualifications
  • Bachelor's Degree in a science or business function
  • 0-2 Years related industry experience in Clinical Trials or Pharmacy
  • 0-2 Years related experience in Clinical Supplies - this could be from Supply Chain, Packaging, Distribution or IRT functions.
  • Ability to demonstrate good project management skills.
  • Ability to create effective working relationships with internal and external stakeholders.
  • Ability to demonstrate effective communication and direction.
  • Ability to problem solve.
  • Good Microsoft Office skills (Word, Excel, Powerpoint etc).
  • Proficient in the English language.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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