Study Start Up Associate II
Clinical Careers Page(11 days ago)
About this role
The Study Start Up Associate II at ICON plays a key role in initiating clinical trials by managing regulatory documentation, liaising with stakeholders, and ensuring compliance with regulatory guidelines. The position involves supporting study teams and improving start-up processes to facilitate clinical research. It is designed for individuals with experience in clinical research or regulatory affairs within the healthcare industry.
Required Skills
- Regulatory Affairs
- Clinical Trials
- ICH-GCP
- Project Management
- Documentation
- Stakeholder Liaison
- Regulatory Submissions
- Process Improvement
- Communication
- Life Sciences
Qualifications
- Bachelor's degree in life sciences or related field
- Minimum of 2 years 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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