Site Activation Lead
About the role
This vacancy has now expired. Please click here to view live vacancies.
- Lead clinical trial start-up activities by understanding the client objectives and assist in the development of the plan for country and site distribution
- Oversees day to day delivery of all aspects of site activation in the projects assigned.
- Ensures that each project has a site activation plan and that the study is being conducted in accordance with that plan and in an effective manner which meets sponsor timelines and expectations and is in compliance with ICON/client KPIs, ICON/client SOPs, reporting norms, appropriate regulations and ICON's quality standards
- lead sponsor initiatives such as kick-off meetings, bid defenses, project update and status calls, and other communications
- Utilize project management skills to optimize performance and collaboration to ensure successful study outcomes
- Bachelor's Degree preferably in life sciences
- Minimum of 5 year of experience in a Clinical Research environment, focusing on Start Up experience
- Project management skill set
- Understanding of regulatory and submission processes in many different countries
- Excellent written and verbal communication
- Ability to work to tight deadlines
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
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Temporary Employee
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR141156
Expiry date
01/01/0001
Author
Zaklina LomberAuthor
Zaklina LomberSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety
Reference
JR141140
Expiry date
01/01/0001
Author
Simone ChanAuthor
Simone ChanSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting t
Reference
JR141136
Expiry date
01/01/0001
Author
Simone ChanAuthor
Simone ChanSalary
Location
Poland, Warsaw
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Warsaw
Lisbon
Bucharest
Barcelona
Tallinn
Reading
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical Writing
Job Type
Permanent
Description
We are currently seeking a Medical Writer II to join our diverse and dynamic team. As a Medical Writer II at ICON, you will play a pivotal role in the development and preparation of clinical trial doc
Reference
JR139524
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
Argentina, Buenos Aires
Department
Clinical Monitoring
Location
Buenos Aires
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
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
JR134522
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Argentina, Buenos Aires
Department
Clinical Monitoring
Location
Buenos Aires
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
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 Specialist at ICON, you will play a pivotal role in designing and an
Reference
JR135211
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia Pistolesi