CTA
Clinical Careers Page(1 month ago)
About this role
A Clinical Trial Administrator at ICON supports clinical research efforts within a global healthcare intelligence and clinical research organization. Based in Mexico City, the role contributes to clinical trial execution and the advancement of innovative treatments by assisting study teams and managing trial-related activities.
Required Skills
- Clinical Trials
- Documentation
- Regulatory Compliance
- Informed Consent
- CRF Preparation
- Communication
- Organization
- Data Analysis
- Collaboration
- Reporting
+1 more
Qualifications
- Bachelor's Degree in Scientific or Healthcare 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.
View more jobs at Clinical Careers Page →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Clinical Careers Page
Similar Jobs
Clinical Research Study Assistant II - Neurology
Washington University in St. Louis(1 month ago)
Assistant(e) de recherche/Research Assistant - Newmarket, ON
IQVIA(1 month ago)
SR CRA I - Sponsor dedicated - Mexico Home Based
Clinical Careers Page(2 months ago)
Clinical Research Coordinator
McKesson(1 month ago)
Sr CRA1
IQVIA(1 month ago)
Research Coordinator
IQVIA(1 month ago)