Clinical Research Associate

Translational Research in Oncology; Paris; À distance; EUR 53 000 - 61 000; Plein temps

Avantages offerts par ce poste

Competitive salary

5 weeks vacation plus ChristmasClosure

Health & Life Insurance premiums paid

Flexible working hours

Home office allowance

Luggage allowance

Mobile phone allowance

Résumé du poste

Translational Research in Oncology (TRIO) seeks an experienced Clinical Research Associate to join our Monitoring Resources team. This home-based role in France reports to a CRA Line Manager and supports oncology trials with adherence to ICH-GCP and regulatory standards.

The position requires monitoring experience, strong ICH-GCP knowledge, and ability to travel up to 60%. TRIO offers competitive salary, generous vacation, and comprehensive benefits.

Qualifications

• A minimum of 2 years of monitoring experience in oncology trials.
• Completion of a science-related Bachelor's degree.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCP knowledge.
• Experience with clinical trial information systems.
• Fluent in French and English.
• Ability to travel up to 60% on average.

Responsabilités

• Conducting site visits, including pre-study, initiation, monitoring and termination.
• Confirming adherence to 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.

Connaissances

Fluent in French and English

ICH-GCP knowledge

Clinical monitoring process knowledge

Clinical trial information systems

Ability to travel 60%

Formation

Science-related Bachelor's degree

Description du poste

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 clinical research organizationdedicated 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 Associateto 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;
• Confirmingadherence 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
• Luggage allowance
• Mobile phone allowance

Pay Range:52,500.00 to61,250.00 Euro -Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, abilities of the applicant, internal equity, and alignment with market data.

Teamwork · Passion · Integrity · Innovation