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Project Manager - NASH (Home-based)

JR064322

About the role

This vacancy has now expired. Please click here to view live vacancies.

At ICON, it's our people that sets us apart.
As a Project Manager within our Cardiovascular/Metabolic team, you will expect to add towards a culture of project group excellence with a focus on process improvement, adding value and exceeding client needs.
You will be the point of contact for designated projects, responsible to deliver successful client relationships, lead cross-functional teams, define project scope, build resource requirements, risk migration strategies, associate action plan and issue resolution. You will lead global trials within a therapeutically aligned team across a variety of complex indications. As a Project Manager, you are involved at the forefront of innovation and drive delivery using your project leadership expertise.
Our projects range from phase II safety and efficacy trials to large scale outcomes mega-trials. You have the support of extraordinary, tenured and experienced leadership whose goal is to help you apply and expand your project management, drug development and therapeutic expertise.

The Role:

  • Run a cross functional project team ensuring all necessary delivery of project training and developing a succession plan for the core team members
  • Manage project study budgets and invoicing procedures according to study contract
  • Report progress of projects to ICON clients and monitor and implement QC activities as necessary
  • Collaborate with business development to ensure we have a dedicated commercial aptitude and work together with internal colleagues and external partners to identify new avenues for growth

Role Requirements:

  • Bachelor's Degree in science, business, medicine or equivalent degree
  • Project Management or equivalent (PMI certification) is desirable
  • At least 2 years PM experience within clinical research and study operations
  • Experience working on NASH studies
  • Comprehensive knowledge of ICH-GCP
  • Strength in communication, planning, decision-making, negotiation, conflict management and time management skills
  • Willingness to travel up to 25% as needed
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Day in the life

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Central Monitoring vs On Site Monitoring

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Publish date

04/03/2026

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Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

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Francis' Journey back to ICON

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03/26/2026

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Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

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Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

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Lydia's Journey Back to ICON

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03/24/2026

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Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv

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Learn about Lydia's return to ICON and why she felt it was a natural choice.

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