Manager, Feasibility and Site Activation - Contracts
- Blue Bell
- Study Start Up
- ICON Full Service & Corporate Support
- Remote or Office
Talent Acquisition Segment Lead
- Full Service Division
About the role
Manager, FSA
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Manager, Feasibility and Site Activation (FSA) at ICON, you will lead teams responsible for delivering high-quality feasibility assessments and efficient site activation for global clinical trials.
What You Will Do:
Your focus will be on coordinating site start-up and activation delivery, resolving issues, and developing team capability.
Key responsibilities include:
- Managing FSA project teams to deliver country and site feasibility, start-up strategies, and activation activities in line with timelines and quality expectations.
- Overseeing the coordination of essential documents, regulatory and ethics submissions, and contract/start-up packages for assigned studies.
- Reviewing feasibility data, assumptions, and risks, and partnering with stakeholders to develop mitigation plans and realistic start-up forecasts.
- Collaborating with business development and operational teams to support proposals, bid defences, and customer meetings with robust FSA input.
- Monitoring performance metrics for feasibility and site activation, identifying trends and driving continuous improvement initiatives.
- Providing coaching, feedback, and development opportunities to FSA staff, fostering a culture of accountability and collaboration.
Your Profile:
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent experience.
- Significant experience in clinical research with a strong focus on feasibility, site selection, and study start-up.
- Proven ability to manage projects or teams in a fast-paced, matrixed environment.
- Strong analytical and planning skills, with experience interpreting feasibility data and operational metrics.
- Excellent communication and stakeholder management skills, including customer-facing experience.
- Continuous improvement mindset, with a focus on quality, predictability, and operational excellence.
- Willingness to travel as required (approximately 15%)
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
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
Similar jobs at ICON
Salary
Location
Hungary, Budapest
Location
Prague
Budapest
Warsaw
Barcelona
Madrid
Gdansk
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatm
Reference
JR153071
Expiry date
01/01/0001
Author
Orsolya BerkeAuthor
Orsolya BerkeSalary
Location
South Africa, Johannesburg
Location
Johannesburg
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
The Role:As a Senior Site Specialist, you will be responsible for completing country and/or regional clinical trial regulatory deliverables in line with study specifics, ensuring compliance with ICH-G
Reference
JR147026
Expiry date
01/01/0001
Author
Jacek JaworskiAuthor
Jacek JaworskiSalary
Location
Poland, Warsaw
Location
Warsaw
Istanbul
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Support Assistant at ICON, you will provide administrative and operational support for clinical trials, contributing to the advancement of innovative treatments and therapies.What You Will
Reference
JR151407
Expiry date
01/01/0001
Author
Jacek JaworskiAuthor
Jacek JaworskiSalary
Location
China, Chengdu
Location
Chengdu
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Job Advert PostingWe are currently seeking a Site Specialist II to join our diverse and dynamic team. As a Site Specialist II at ICON, you will play a pivotal role in designing and analyzing clinical
Reference
JR146789
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Mexico, Mexico City
Department
Full Service - Development & Commercialisation Solutions
Location
Mexico City
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Start Up Associate I at ICON, you will facilitate the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute to the advancement of innovative treatm
Reference
JR151942
Expiry date
01/01/0001
Author
Daniela GuerreroAuthor
Daniela GuerreroSalary
Location
Spain, Barcelona
Location
Barcelona
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Site Specialist II to join our diverse and dynamic team. As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key o
Reference
JR147222
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda Kozuszek