Clinical Research Associate 1 at Fortrea

Paris, Ile-de-France, France -

Full Time

Start Date

Immediate

Expiry Date

30 Jun, 26

Salary

0.0

Posted On

01 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Management, Monitoring, Data Integrity, Informed Consent, Adverse Event Reporting, CRF Review, Query Generation, Training, Mentoring, Data Review, Regulatory Compliance, Patient Safety, Documentation, Communication, Teamwork, Problem Solving

Industry

Biotechnology Research

Description

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 Driver's License. Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Responsibilities

The Clinical Research Associate 1 is responsible for all aspects of site management as outlined in project plans, including on-site monitoring and ensuring compliance with regulatory requirements. They will also monitor data integrity and assist in training new employees.