Site Management Associate II
Clinical Careers Page(1 month ago)
About this role
The Site Management Associate II at ICON supports clinical research by facilitating the management and oversight of clinical trial sites. Based in Mexico City, this role contributes to ensuring study conduct aligns with regulatory standards and the company's clinical development objectives.
Required Skills
- Site Management
- Clinical Monitoring
- GCP
- Regulatory Compliance
- Project Management
- Data Analysis
- Communication
- Stakeholder Management
- Training
- Mentoring
+1 more
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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