(SR) Internal Medicine & Immunology Project Manager
About the role
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At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
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.
Are you ready to be a part of a successful study delivery team? ICON's award-winning study execution capabilities have led to the approval of 18 of the world's top 20 best-selling drugs. Make your experience count for the benefit of patients worldwide.
Location: Any US location (Home or Office Based)
At ICON, it's our people that sets us apart.
As a Project Manager on our Internal Medicine and Immunology 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.
Dermatology is a high priority area for ICON. We have established a Dermatology Centre of Excellence (CoE) and we are looking for Project Managers with dermatology experience to join our team; we are specifically looking for Project Managers with Atopic Dermatitis, Psoriasis, Hidradenitis suppurativa and other dermatology indications experience, preferably in multicountries phase 2 and 3 studies.
Our Internal Medicine and Immunology team covers a broad and varied range of Therapeutic areas including Gastrointestinal, Respiratory, Dermatology, Immunology, Urology & Ophthalmology.
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
- Subject matter expertise in (insert therapeutic area)
- 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.
#LI-JC2
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. Learn more about Our Culture at ICON
Day in the life
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12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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