Sr. Clinical Trial Manager - CNS/Rare Diseases (Home-based)
About the role
This vacancy has now expired. Please click here to view live vacancies.
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?
At ICON, we have an incredible opportunity for an expert Sr. Clinical Trial Manager to join the team in the US.
The Role:
The Sr. Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities. The CTM will also participate in Sponsor, Investigator and bid defense meetings.
What you need:
- 4 year degree or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in CNS and/or Rare Diseases
- Prior monitoring experience is preferred
- Ability to travel up to 20%
- Fluent in local language - both written & verbal
Why join us?
Other than working with an outstanding team of ambitious people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
Ongoing development is vital to us, and as a Clinical Trial Manager, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international and we sincerely 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
Explore more about ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Meet the CRA helping shape a new partnership Ask Rebeca Rojas Hernández what her dad tells people she does for a living and she can't help but smile. "He proudly tells everyone that I visit clinic
Teaser label
Our PeopleContent type
BlogsPublish date
07/06/2026
Summary
Inside the Role of a Senior CRA: Diego's Clinical Research Career at ICON Ask Diego Prieto what he does for a living and his answer is refreshingly simple. "I usually tell people I work on trial
Teaser label
Inside ICONContent type
BlogsPublish date
07/06/2026
Summary
Why returning to ICON was the right career move for Albert Bekfi Sometimes the next step in your career means moving on. Sometimes it means coming back. For Albert Bekfi, Vice President, Pharmacov
Similar jobs at ICON
Salary
Location
Ireland, Dublin
Department
Full Service - Corporate Support
Location
Dublin
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Accounting & Finance
Job Type
Permanent
Description
As a Director, Financial Business Partnering at ICON, you will drive financial strategy and decision-making across the organization. What You Will Do:You will lead finance and financial management del
Reference
JR155677
Expiry date
01/01/0001
Author
Damien KehirAuthor
Damien KehirSalary
Location
Portugal, Lisbon
Location
Lisbon
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:You will
Reference
JR156079
Expiry date
01/01/0001
Author
Lola PomboAuthor
Lola PomboSalary
Location
China, Shanghai
Department
Language Services
Location
Shanghai
Tokyo
Seoul
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Technical Project Management
Non-Clinical Project Management
Job Type
Permanent
Description
As an Associate Project Manager at ICON, you will support the coordination and management of clinical trials, contributing to the design, analysis, and advancement of innovative treatments and therapi
Reference
JR151426
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Poland, Warsaw
Location
Sofia
Warsaw
Johannesburg
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Technical Project Management
Non-Clinical Project Management
Job Type
Permanent
Description
The eCOA UAT Lead member is a key member of the eCOA Solutions team. The eCOA Application specialist acts as the ICON expert that approves the design of eCOA Systems and creates appropriate testing pl
Reference
JR149987
Expiry date
01/01/0001
Author
Clodagh FinneganAuthor
Clodagh FinneganSalary
Location
Turkey, Istanbul
Location
Istanbul
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:You will
Reference
JR155637
Expiry date
01/01/0001
Author
Tuba SuAuthor
Tuba SuSalary
Location
Austria, Vienna
Location
Vienna
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR154471
Expiry date
01/01/0001
Author
Sarah CameronAuthor
Sarah Cameron