Site and SSU Specialist
Clinical Careers Page(1 month ago)
About this role
A Site and Study Start Up Specialist at ICON plc will be part of a clinical research organization supporting the initiation and activation of clinical trials. The role sits within a multidisciplinary team contributing to the timely and compliant start-up of studies and supporting ICON’s clinical development mission.
Required Skills
- Regulatory Submissions
- Ethics Committees
- Stakeholder Liaison
- Record Management
- Project Management
- ICH-GCP
- Communication Skills
- Process Improvement
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.
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