Study Start Up Associate II
Clinical Careers Page(11 days ago)
About this role
ICON plc is seeking a Study Start Up Associate II to lead the initiation of clinical trials by managing regulatory submissions, coordinating approvals, and supporting study teams to ensure compliance and efficiency in clinical research.
Required Skills
- Regulatory Affairs
- Clinical Trials
- Documentation
- Project Management
- Communication
- Stakeholder Management
- ICH-GCP
- Regulatory Submissions
- Clinical Research
- 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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