Remote Oncology Clinical Research Associate (France)

Translational Research in Oncology; Paris; Ibrido; EUR 52.500 - 61.250; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

5 weeks vacation + Christmas closure

Health & Life Insurance premiums paid

Flexible working hours

Home office allowance

Luggage allowance

Mobile phone allowance

Descrizione del lavoro

Translational Research in Oncology (TRIO) is seeking an experienced Clinical Research Associate to join our Monitoring Resources team. This role is home-based in France and reports to a CRA Line Manager.

The candidate will conduct site visits, ensure regulatory compliance, verify data, and support budget and mentoring activities. Qualified applicants have 2+ years of oncology monitoring, fluent French and English, a science-related Bachelor's degree, strong ICH‑GCP knowledge, and experience with

Competenze

• 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‑GCP knowledge.
• Experience with clinical trial information systems.
• Ability to travel up to 60% on average.

Mansioni

• Conduct site visits including pre-study, initiation, monitoring and termination.
• Confirm adherence to FDA, ICH‑GCP and local regulations.
• Ensure completion and collection of regulatory documents.
• Perform data verification of source documents.
• Ensure implementation and compliance with FDA, ICH‑GCP guidelines.
• Participate in budget negotiation and follow-up where applicable.
• Assist with data validation and query resolution.
• Mentor junior team members as required.

Conoscenze

Oncology monitoring

French & English

ICH-GCP knowledge

Medical terminology

Clinical trial systems

Travel up to 60%

Formazione

Bachelor's degree in science

Strumenti

Clinical trial information systems

Descrizione del lavoro

Monitoring Resources - Normandy, Ile-de-France, France - Full Time

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:

• 5 weeks of vacation plus paid Christmas Closure
• Health& Life Insurance premiums respectively paid 50% & 100% by TRIO
• Home office 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.

If you are interested, please submit your resume in English.We thank all candidates for their interest; only those selected for an interview will be contacted.

To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.

To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.