Senior Study Start-up Associate
Clinical Careers Page(4 days ago)
About this role
ICON plc is a leading healthcare organization that specializes in clinical research and development. They are seeking a Senior Study Start Up Associate to support the initiation and setup of clinical trials, ensuring regulatory compliance and smooth project execution. The role involves working within a fast-paced environment to facilitate study start-up activities across countries and sites.
Required Skills
- feasibility
- Regulatory Compliance
- Informed Consent
- Site Identification
- Contract Negotiation
- Clinical Trials
- Study Start Up
- GCP
- Regulatory Submissions
- Patient Safety
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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