Remote Oncology Clinical Research Associate (France)

Translational Research in Oncology

Paris

Sur place

EUR 52 500 - 61 250

Plein temps

14 jours+

Générateur de candidature

Obtenez une réponse de cet employeur — un CV et une lettre de motivation adaptés exactement à ce qu’il recherche.

Passez les filtres ATS

Avantages offerts par ce poste

Competitive salary

5 weeks vacation + Christmas closure

Health & Life Insurance premiums paid

Flexible working hours

Home office allowance

Luggage allowance

Mobile phone allowance

Résumé du poste

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

Qualifications

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.

Responsabilités

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.