Sr. Study Start Up Associate (ICF Reviewer) - Home-Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
Sr. Study Start Up Associate (Informed Consent) - Home-based Any where in US
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
We are looking for someone with Informed Consent Form review experience (ICF Reviewer) to join our Study Start Up group. Our Study Start Up associates are integral in ensuring that physicians at research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices.
The role
- Your main role is to review Informed Consent Forms and negotiate language as needed
- You will review and negotiate these changes and potentially liaise with other stakeholders like the sponsor, legal, or the clinical team to ensure that changes to the ICF are acceptable.
- You will assist in the drafting of ICF country templates for the United States and Canada, which are then distributed to study sites to make edits depending on their local IRB requirements and SOPs
What you need
- Associates who have a background in clinical research at a CRO, Pharmaceutical company, study site, or who have worked at an IRB
- Performing ICF review as an essential function of the job for a minimum 3+ years
- Bachelor's degree in the life sciences is preferred
Why join us?
Ongoing development is vital to us, and as a Study Start Up Associate you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin
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
Teaser label
Our PeopleContent type
BlogsPublish date
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
Similar jobs at ICON
Salary
Location
UK, Reading
Location
Sofia
Lisbon
Bucharest
Barcelona
Madrid
Tallinn
Reading
Gdansk
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer II to join our diverse and dynamic team. As a Senior Statistical Programmer II at ICON, you will play a vital role in the analysis and reportin
Reference
JR139390
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
France, Paris
Department
Clinical Monitoring
Location
Paris
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
ICON plc is a global healthcare intelligence and clinical research organization, committed to innovation, excellence, and inclusion. Join our mission to advance clinical development across a broad ran
Reference
JR138394
Expiry date
01/01/0001
Author
Sophie ClarkeAuthor
Sophie ClarkeSalary
Location
Czech Republic, Prague
Location
Prague
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR139257
Expiry date
01/01/0001
Author
Jaroslav PolákAuthor
Jaroslav PolákSalary
Location
Germany, Frankfurt
Location
Sao Paulo
Bogota
Mexico City
Frankfurt
Madrid
Manila
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
Job Advert Missing
Reference
JR139162
Expiry date
01/01/0001
Author
Sarah CameronAuthor
Sarah CameronSalary
Location
US, Lenexa KCIB (PRA)
Department
Full Service - Quality Assurance
Location
Lenexa
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
We are currently seeking a Quality Assurance Auditor II to join our diverse and dynamic team at our bioanalytical lab in Lenexa, Kansas. As a Quality Assurance Auditor II at ICON, you will play a pivo
Reference
JR134930
Expiry date
01/01/0001
Author
Meris MyersAuthor
Meris MyersSalary
Location
France, Paris
Location
Paris
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate I or II to join our diverse and dynamic team in a sponsor dedicated role. As a Clinical Research Associate at ICON, you’ll be a key part of runni
Reference
JR135711
Expiry date
01/01/0001
Author
Sophie ClarkeAuthor
Sophie Clarke