Match score not available

Clinical Trial Supply Chain Manager (Remote/Home-Based)

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Brazil, Argentina, Peru, Mexico

Offer summary

Qualifications:

Bachelor's Degree in science or business (not mandatory), 2-3 Years related experience in Clinical Trials, 2-3 Years experience in Clinical Trial Supply Chain Management, Good project management skills, Strong Microsoft Office and IRT/IXRS skills.

Key responsabilities:

Interpret clinical trial protocols for planning
Create master English label text per regulations
Maintain demand forecasts and packaging plans
Set up and monitor Interactive Response Technology systems
Provide budget tracking for efficient project management

IQVIA Italia SME https://www.iqvia.com/

10001 Employees

See more IQVIA Italia offers

Job description

Job Summary

The Clinical Supply Chain Manager is responsible for the strategic planning and execution of new clinical trial supply chains. This involves the ability to interpret a clinical trial protocol in conjunction with other key study information to create an appropriate kit design and formulate a strong supply plan. The Clinical Supply Chain Manager will lead internal and external partners, to ensure delivery of the supply plan in accordance with study timelines.

You will:

Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution.
Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13)
Create and 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.
Setup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed.
Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it.
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.
Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations.

What do you need to have:

Bachelor's Degree in a science or business function (Not mandatory)
2-3 Years related industry experience in Clinical Trials (Essential).
2-3 Years experience in Clinical Trial Supply Chain Management (Essential).
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.
Strong Microsoft Office skills and IRT/IXRS.
Proficient Level of English.

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