Clinical Supply Specialist

Posted 10 Days Ago
Be an Early Applicant
Hiring Remotely in Milan, ITA
In-Office or Remote
Entry level
Pharmaceutical
The Role
Supports clinical trial supply operations across EU and US markets, including demand and supply planning, forecasting, resupply parameters, IRT/RTSM setup and maintenance, UAT coordination, shipment oversight, inventory tracking, expiry and lot management, reconciliation, KPI reporting, and issue resolution. Collaborates with depots, couriers, packaging and labeling partners, IRT vendors, and internal stakeholders while ensuring GMP compliance and effective handling of deviations and temperature excursions.
Summary Generated by Built In

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Clinical Supply Chain to join a pharmaceutical company

ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counterparts.  

 

Main Job Tasks and Responsibilities:

 

Within the Clinical Supply Unit, we are looking for an experienced operational resource who can directly support day-to-day clinical supply execution and coordination across EU and US, with strong working knowledge of GMP, IRT/RTSM, distribution, and shipment oversight.


  • Study supply planning support: demand/supply planning, forecasting support, resupply parameters, scenario planning, and risk mitigation
  • IRT/RTSM operational support: requirements gathering, set-up support with vendor, UAT coordination, change management, and ongoing maintenance support
  • Shipment execution and oversight (EU and US): depot-to-site and site-to-site shipments, temperature-controlled logistics as needed, shipment tracking, issue resolution, and documentation
  • Supply tracking and reporting: inventory monitoring, expiry/lot management, reconciliation support, and regular KPIs/status reporting
  • Close collaboration with internal stakeholders and external vendors (depots, couriers, packaging/labeling partners, IRT provider), ensuring timely follow-up and proactive problem-solving
  • Geographic scope: EU and US (supporting a global study supply operation)
  • Working model: remote/hybrid acceptable; occasional travel may be required (to be defined)

Education and Experience:


  • Bachelor's degree
  • Proven experience in clinical trial supply operations (phases [I/II/III], multi-country)
  • Strong familiarity with GMP and IRT/RTSM workflows (set-up support, UAT, change controls, releases, and ongoing operations)
  • Solid understanding of global distribution and logistics (incl. EU/US), import/export basics, temperature excursions management and deviation handling
  • Strong organizational skills, ability to manage multiple priorities under tight timelines, and clear stakeholder communication
  • Fluency in English; additional languages are a plus


The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

 

Who will you be working for?


About ClinChoice    

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical devices, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           


Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are  the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.


Key words: Clinical Supply Specialist, planning, supply planning, demand, demand planning, forecasting, resupply parameters, risk mitigation, IRT, RSTM, UAT, shipment, depot to site, site to site, logistic, inventory, inventory monitoring, packaging, labeling, GMP, English, Clinical Trials, CRO, Clinical Research Organization, Clinical Research, , Outsourcing, Contract, Temporary, CRO, Contract Research Organisation, Outsourced, Outsourcing, Sponsor-dedicated


#LI-RE1 #LI-REMOTE #TEMPORARY #FUL TIME

Skills Required

  • Bachelor's degree
  • Proven experience in clinical trial supply operations across Phase I, II, and III, including multi-country studies
  • Strong familiarity with GMP and IRT/RTSM workflows, including setup support, UAT, change controls, releases, and ongoing operations
  • Understanding of global distribution and logistics across the EU and US
  • Knowledge of import/export basics, temperature excursion management, and deviation handling
  • Strong organizational skills and ability to manage multiple priorities under tight timelines
  • Clear stakeholder communication skills
  • Fluency in English
  • Additional language proficiency

ClinChoice Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

ClinChoice Insights

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The Company
HQ: Fort Washington, PA
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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