- Prepare, review contract negotiation with external sites in Germany, working to project deadline to finalise study contracts
- You will be collaborating with multiple internal and external teams to coordinate the contract templates and budgets throughout the timeframe
- Completing contract amendment activities
- Other study start up activities as required including: ethics submissions, creating submissions packages, amendments to study documentation according to country guidelines
- Bachelor’s Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline
- Global clinical trials experience with awareness of global regulatory requirements for clinical site initiation documents
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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BlogsPublish date
01/26/2026
Summary
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BlogsPublish date
01/20/2026
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BlogsPublish date
01/05/2026
Summary
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Salary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office or Home
Job Categories
Project/ Program Management
Resourcing
Job Type
Permanent
Description
We are currently seeking a Resource Planning Specialist to join our diverse and dynamic team. As a Resource Planning Specialist at ICON, you will play a key role in supporting project risk management
Reference
JR142806
Expiry date
01/01/0001
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Salary
Location
Miami, FL
Location
Miami, FL
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What will you be doing?Works on multiple trials within the Cross Therapeutic areas - Start up focus Collaborate with country operations teams to identify, select, and activate clinical trial sites in
Reference
JR142765
Expiry date
01/01/0001
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Salary
Location
New Jersey
Location
New Jersey
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing:Serve as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and clo
Reference
JR142762
Expiry date
01/01/0001
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Salary
Location
Ohio
Location
Ohio
Indianapolis, IN
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What will you be doing?Works on multiple trials within the Cross Therapeutic areas - Start up focus Collaborate with country operations teams to identify, select, and activate clinical trial sites in
Reference
JR142768
Expiry date
01/01/0001
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Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You’ll Be Doing:Serve as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and close
Reference
JR142270
Expiry date
01/01/0001
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Salary
Location
Minnesota
Location
Minnesota
Remote Working
Remote
Job Categories
Study Start Up
Job Type
Permanent
Description
Through coordination with the Contract & Budget team, and collaboration with divisional and regional clinical teams, the SSU Associate II conducts clinical trial site start-up activities related to th
Reference
JR141979
Expiry date
01/01/0001
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