Clinical Research Associate

Description

If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in France.

Responsibilities:

Conducting site visits, including pre-study, initiation, monitoring and termination;

Confirming adherence to all FDA, ICH-GCP and local regulations;

Ensuring the completion and collection of regulatory documents;

Performing data verification of source documents;

Ensuring implementation and compliance with FDA, ICH-GCP guidelines;

Participating in budget negotiation and follow-up where applicable;

Assisting with data validation and query resolution;

Mentoring junior team members as required.

Qualifications:

A minimum of 2 years of monitoring experience in oncology trials

Fluent in French and English

Completion of a science-related Bachelor’s degree

Excellent knowledge of medical terminology and clinical monitoring process

Strong ICH-GCPs knowledge

Experience with clinical trial information systems

Ability to travel up to 60% on average

What TRIO Can Offer You:

Competitive salary

5 weeks of vacation plus paid Christmas Closure

Health & Life Insurance premiums respectively paid 50% & 100% by TRIO

Flexible working hours

Home office allowance

All interviews are currently being conducted virtually - via phone or video. We thank all candidates for their interest; only those selected for an interview will be contacted.