Site Management Associate II
Clinical Careers Page(1 month ago)
About this role
Site Management Associate II at ICON plc supporting the management and monitoring of clinical trial sites in Mexico City. The role helps ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice while fostering relationships with site personnel and supporting site management teams to improve clinical research operations.
Required Skills
- Site Management
- Clinical Monitoring
- GCP
- Regulatory Compliance
- Project Management
- Data Analysis
- Communication
- Mentoring
Qualifications
- Bachelor's Degree in Life Sciences or Related Field
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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