Remote Oncology CRA - France Based, Travel Up to 60%

TRIO - Translational Research in Oncology

Paris

Sur place

EUR 52 500 - 61 250

Plein temps

14 jours+
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

Passez les filtres ATS

Avantages offerts par ce poste

5 weeks vacation
Health & Life Insurance premiums paid
Flexible working hours
Home office allowance
Luggage allowance
Mobile phone allowance

Résumé du poste

TRIO - Translational Research in Oncology is seeking an experienced Clinical Research Associate to join the Monitoring Resources team. This home-based role in France requires at least 2 years of oncology trial monitoring experience and fluency in French and English.

You will conduct site visits, ensure regulatory compliance, manage documents, verify data, and support budgets. Travel up to 60% and mentoring duties are included in the role.

Qualifications

  • Minimum 2 years of oncology trial monitoring experience.
  • Fluent in French and English.
  • Bachelor’s degree in a science‑related field.
  • Strong knowledge of ICH‑GCP.
  • Experience with regulatory documents and data verification.
  • Willingness to travel up to 60%.

Responsabilités

  • Conduct site visits (pre‑study, initiation, monitoring, termination).
  • Ensure adherence to FDA, ICH‑GCP and local regulations.
  • Collect and complete regulatory documents.
  • Verify data against source documents.
  • Implement ICH‑GCP guidelines and FDA requirements.
  • Assist with budget negotiation and follow‑up where applicable.
  • Support data validation and resolve queries.
  • Mentor junior team members.

Connaissances

Monitoring experience
Fluent French & English
Travel up to 60%

Formation

Science-related Bachelor’s degree

Outils

Clinical trial information systems

Description du poste

TRIO - Translational Research in Oncology is seeking an experienced Clinical Research Associate to join the Monitoring Resources team. This home-based role in France requires at least 2 years of oncology trial monitoring experience and fluency in French and English.

You will conduct site visits, ensure regulatory compliance, manage documents, verify data, and support budgets. Travel up to 60% and mentoring duties are included in the role.

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