Site Management Associate II
Clinical Careers Page(1 month ago)
About this role
The Site Management Associate II supports the management and monitoring of clinical trial sites, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice. The role contributes to clinical research operations efficiency and fosters strong relationships with site personnel and cross-functional teams.
Required Skills
- Site Monitoring
- Regulatory Compliance
- GCP
- Project Management
- Data Analysis
- Documentation
- Communication
- Mentoring
- Relationship Building
- Time Management
Qualifications
- Bachelor's Degree in Life Sciences, Healthcare Administration, or Clinical Research
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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