Clinical Research Associate 1

Paris - France

Monthly Salary: Not Disclosed

Posted on: 2 days ago

Vacancies: 1 Vacancy

Job Summary

Fortrea is growing his FSO department! We are actively looking for a CRA I to join our team.

Responsibilities:

Responsible for all aspects of site management as prescribed in the project plans.
General On-Site Monitoring Responsibilities.
Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
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.
Track and follow-up on Serious Adverse Event (SAE) reporting process production of reports narratives and follow up of SAEs.
Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management.
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
Works efficiently and effectively in a matrix environment.
Valid Drivers License.

Learn more about our EEO & Accommodations request here.

Required Experience:

Fortrea is growing his FSO department! We are actively looking for a CRA I to join our team.Responsibilities:Responsible for all aspects of site management as prescribed in the project plans.General On-Site Monitoring Responsibilities.Ensure the study staff who will conduct the protocol have receive...