Study Start Up Associate
Clinical Careers Page(9 days ago)
About this role
A Study Start Up Associate II at ICON plays a key role in initiating clinical trials by managing regulatory submissions and coordinating with stakeholders. The position involves ensuring compliance with regulatory standards and supporting process improvements to facilitate study start-up activities.
Required Skills
- Regulatory Submissions
- Clinical Trials
- GCP
- Project Management
- Stakeholder Liaison
- Documentation
- Process Improvement
- Clinical Research
- Regulatory Affairs
- IRB
Qualifications
- Bachelor's degree in life sciences or related field
- 2+ years of experience in clinical research or regulatory affairs
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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