Clinical Research Associate I

Fortrea is looking for CRA I to join FSO department.

You Responsibilities (but not only):

• 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.

Experience:

• 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 problem-solving skills.
• Valid Driver's License.

Learn more about our EEO & Accommodations request here.