TRIO is a leading oncology clinical research organization (CRO) dedicated to accelerating drug development through translational research. With decades of experience conducting comprehensive oncology trials from inception to completion, TRIO leverages a global network of investigators and academic leaders to bring innovative therapies to clinics on the most rational path. Focused on saving lives with efficiency and care, they deliver targeted concepts with a commitment to excellence.
Open Positions
Clinical Research Physician
Medical Doctor degree, at least 1 year of experience in medical monitoring in oncology trials, and knowledge of ICH GCP guidelines required
Computer Systems Validation Assistant
Intermediate to Advanced proficiency with Microsoft Office applications, Excellent attention to detail, Self-starter with the ability to work independently as well as collaboratively within a team
Clinical Research Physician
1+ year of experience in medical monitoring in oncology trials, MD degree, ICH GCP guidelines knowledge
Clinical Research Physician
Medical Doctor degree, at least 1 year of experience in medical monitoring in oncology trials, current knowledge of ICH GCP guidelines
Clinical Research Physician
Medical Doctor degree, 1 year of experience in medical monitoring in oncology trials, and excellent knowledge of ICH GCP guidelines
Senior Clinical Research Associate
2+ years monitoring experience, 5+ years CRA experience, fluency in English, Bachelor's degree in science
Clinical Research Associate
2 years of monitoring experience in oncology trials and a science-related Bachelor's degree required
Clinical Research Associate
At least 2 years of monitoring experience, early-phase trials experience, Bachelor's degree in a science-related field, strong ICH-GCPs knowledge
Clinical Research Associate
2+ years of monitoring experience in oncology trials, completion of a science-related Bachelor's degree, and excellent knowledge of medical terminology
Clinical Research Physician
Medical Doctor degree, 1 year of experience in medical monitoring in oncology trials, current knowledge of ICH GCP guidelines
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