Job Details

Science is seeking a Clinical Research Associate (CRA) to lead start-up, monitoring, and close-out of US trials, ensuring subject safety and data integrity. The role serves as the main liaison with trial sites, ensuring adherence to protocol, FDA regulations, ISO 14155, and internal SOPs while identifying process improvements.

Travel up to 40% across the United States and occasional abroad is expected. Strong technical writing and CTMS/EDC proficiency are required to succeed.