Please note: This position is only considering candidates that can work out of our Durham, NC office. This is an In house CRA position
Conduct site management and data monitoring of assigned clinical sites. Ensure that all activities are conducted in accordance with applicable Good Clinical Practices (GCP) and Standard Operating Procedures (SOP).
Education and Experience
Bachelor’s degree, preferable in science or in a related field. 3 years of previous CRA or advanced clinical data experience. Experience monitoring clinical trials in oncology is required, HCC experience preferred. Real world evidence or phase IV experience preferred.
Knowledge, Skills, and Abilities
Excellent knowledge of Good Clinical Practice (GCP) in conduct of clinical studies. Excellent written and verbal communication skills. Excellent Microsoft Office skills as well as computer data acquisition and report writing. Ability to interact with all levels of internal and external contacts. Ability to independently set and manage multiple priorities. Ability to demonstrate advanced judgment and decision-making ability in the execution / oversight of study sites.
This is an office-based position. Most monitoring activities are completed remotely, however occasional travel may be required.
Applicants must be authorized to work in the United States without sponsorship. This position is only considering candidates that can work out of our Durham, NC office.
Job Type: Full-time