Job Description
Join Precision for Medicine, where you will be responsible for monitoring and owning the progress of clinical studies at investigative sites, ensuring they align with protocols, SOPs, ICH-GCP, and regulations. You will coordinate study setup, identify investigators, and help prepare regulatory submissions. Senior CRAs manage appropriately sized clinical trials and support Project Managers on larger trials. You will interact with clients, initiate payments, and participate in proposal activities. As a member of our team, you will have a lower than average number of protocols, allowing you to be a protocol expert. We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies.
About Precision for Medicine
Precision for Medicine is a precision medicine Clinical Research Organization that integrates clinical trial execution with scientific knowledge and data sciences.