Site and SSU Specialist
Clinical Careers Page(1 month ago)
About this role
A Site and Study Start Up Specialist at ICON supports the initiation phase of clinical trials within a global clinical research organization, enabling timely study activation and adherence to applicable standards. The role contributes to advancing clinical development programs by coordinating activities across internal and external stakeholders.
Required Skills
- Regulatory Submissions
- Ethics Submissions
- Stakeholder Liaison
- Record Keeping
- Project Management
- ICH-GCP
- Communication
- Process Improvement
- Clinical Research
Qualifications
- Bachelor's Degree in Life Sciences
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
SSU Associate Director
American Association of Physicists in Medicine(5 days ago)
Site Activation Specialist (SSU/RSU)(Evergreen)
IQVIA(1 year ago)
Analista de Ativacao de Estudos Clínicos Sr (Study Start up Lead - SSUL)
Roche(1 month ago)
SSU Site Manager
IQVIA(1 month ago)
Site Activation Partner III - FSP
Parexel(1 month ago)
Site Activation Specialist - The Netherlands
Clinical Careers Page(2 months ago)