Study Start Up Specialist
Clinical Careers Page(13 days ago)
About this role
The Study Start Up Specialist at ICON plays a key role in supporting the initiation of clinical trials, including activities such as feasibility assessments, site identification, and regulatory submissions. The position involves ensuring compliance with regulations and contributing to patient safety through informed consent processes. It operates within a fast-paced, global healthcare research environment.
Required Skills
- Regulatory Compliance
- Clinical Trials
- Site Identification
- Informed Consent
- Feasibility Assessments
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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