Clinical Research Associate I

Job description

Fortrea is looking for CRA I to join FSO department. Experience: Learn more about our EEO & Accommodations request here . - Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. - Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. - Monitor data for missing or implausible data. - Ensure audit readiness at the site level. - Travel, including air travel, may be required and is an essential function of the job. - Participate in and follow-up on Quality Control Visits (QC) when requested.. - Track and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs. - Assist with training, mentoring and development of new employees, e.g., co-monitoring. - Six (6) months experience in a related role. - Fluent in English, both written and verbal. - Basic understanding of Regulatory Guidelines. - Ability to work within a project team. - Good planning, organization, and prob...