Clinical Research Associate I

Paris - France

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

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 Drivers License.

Learn more about our EEO & Accommodations request here.

Required Experience:

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 oth...