Central Services Specialist - ICF
- United States
- Clinical Trial Support
- ICON Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
The Central Services Specialist - ICF Management position will be responsible for review, coordination and finalization of Global Informed Consent Form templates for all clinical studies that are managed by Development Operations. Responsibilities also include supporting CSS Central Services team as needed.
- Co-manages maintenance of the centralized Informed Consent Form mailbox.
- Reviews and validates quality and accuracy of Informed Consent Form templates.
- Supports development of Informed Consent Form templates.
- Responsible for tracking progress of Informed Consent Form template language reviews and escalations.
- Edits and reviews Informed Consent Form templates per protocol while ensuring adherence to Incyte standards and study timelines.
- Assist in the reporting of Key Performance Indicators and Central Services metrics.
- Maintains consistent communications with internal clients, including in-person discussion, telephone calls, and email.
- Bachelor’s Degree in business administration, finance, science or related field or equivalent experience.
- Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.
- Minimum of three years negotiating US Site contracts and budgets.
- Experience in negotiating vendor contracts/budgets.
- Excellent negotiation skills.
- Experience with conflict resolution.
- Proven ability to effectively manage change.
- Ability to negotiate complex contract and payment terms.
- Flexibility to assume a workload which frequently necessitates an adjustment of priorities.
- Goal oriented, self-starter with proven ability to work independently.
- Proactively identify issues and provide potential solutions for resolution.
- Detail oriented.
- Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.
- Proficiency with all applications of Microsoft Office.
- Good interpersonal skills.
- Comfort with ambiguity; ability to act without having the total picture.
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, 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.
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
.jpg)
Teaser label
Inside ICONContent type
BlogsPublish date
01/17/2025
Summary
Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are
.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv

Teaser label
Career ProgressionContent type
BlogsPublish date
07/20/2023
Summary
Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic
Similar jobs at ICON
Salary
Location
United States
Department
Clinical Operations Roles
Location
United States
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Medical Data Reviewer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120040
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Spain
Department
Clinical Operations Roles
Location
Spain
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a SSU Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120307
Expiry date
01/01/0001
Author
Lola PomboAuthor
Lola PomboSalary
Location
Poland, Bulgaria, Spain, Romania, Hungary, Portugal, Italy, Czech Republic
Department
Clinical Operations Roles
Location
Bulgaria
Czech Republic
Hungary
Italy
Poland
Portugal
Romania
Spain
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Excellent new opportunity at ICON on a global FSP program sponsor dedicated to a big global pharmaceutical. We are looking for an Global Study Manager/Associate Project Manager to join a growing and
Reference
2025-119675
Expiry date
01/01/0001
Author
Tanzina GuerniAuthor
Tanzina GuerniSalary
Location
Regional United States (PRA)
Department
Clinical Monitoring
Location
Multiple US Locations
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. The In-House Clinical Research Associate is responsible for managing, implementing and mo
Reference
JR132046
Expiry date
01/01/0001
Author
Jasmine GarciaAuthor
Jasmine GarciaSalary
Location
Sofia
Department
Clinical Operations Roles
Location
Sofia
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Research Associate II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119882
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
Sofia
Department
Clinical Operations Roles
Location
Sofia
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119878
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz Sternlicht