iconplc - Mexico, Remote work

Principal CRA opportunity with ICON plc, home-based in Mexico. Lead complex clinical trials, mentor CRAs, and ensure ICH-GCP compliance across site management activities. Requires a Bachelor’s in a scientific field, extensive CRO/pharma experience, and strong leadership skills. Enjoy competitive ...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Lead pharmacovigilance safety initiatives at a global clinical research leader. Oversee a team ensuring regulatory compliance and risk management for clinical trials in Mexico City. Requires a life sciences degree and significant drug safety experience. We offer competitive health insurance and r...

Join ICON plc in Mexico City as a Senior Clinical Data Science Programmer. Utilize your advanced SAS, R, or Python skills to develop programming solutions for clinical trial data analysis and reporting. You will ensure data accuracy and efficiency in a collaborative, cross-functional environment....

Join ICON plc as a Study Start Up Associate II in Mexico City (home-based). Lead clinical trial initiation, ensure regulatory compliance (ICH-GCP), and manage document submissions. Requires 2+ years in clinical research/regulatory affairs. Enjoy health insurance, competitive retirement plans, and...

Join ICON plc, a global clinical research leader, in Mexico City. As a Clinical Associate, you will support the design and management of clinical trials, advancing innovative therapies. The role requires a Life Sciences degree, clinical research experience, and strong organizational skills. We of...

Join ICON plc as a Senior Clinical Research Associate in Mexico City. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% domestic travel. Enjoy competitive benefits including ...

Join ICON plc as a Clinical Research Associate II in Mexico City. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% domestic travel. We offer competiti...

Lead global clinical trials from Mexico City as a Senior Clinical Trial Manager with ICON. Utilize your 7+ years of CTM experience, including expertise in North America and LATAM studies, to oversee budgets, drive enrollment, and ensure study integrity. Enjoy competitive benefits while shaping th...