Senior Project Manager
- Raleigh
- Clinical Project Management
- ICON Full Service & Corporate Support
About the role
This vacancy has now expired. Please click here to view live vacancies.
Location: Any US location (Home or Office Based)
At ICON, it’s our people that sets us apart.
Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.
As a Senior Project Manager on our Medical Device & Diagnostic Research 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 feasibility and analytical studies to large scale clinical performance and real world evidence trials. You have the support of extraordinary, tenured and experienced leadership whose goal is to help you apply and expand your project management, device 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 certification or equivalent (PMP) is desirable
- At least 2 years PM experience within clinical research and study operations
- Subject matter expertise in Medical Device, specifically In Vitro Diagnostic products
- Experience in supporting proposal development including study budgets for new business opportunities
- 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
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life

Teaser label
Career ProgressionContent type
BlogsPublish date
02/17/2023
Summary
Clinical Trial Managers and Clinical Project Managers are an integral part of the clinical market. Each role is essential in ensuring that clinical trials are well run and completed to a high stan
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