Clinical Research Associate
Translational Research in Oncology
- Paris
- CDI
- Temps-plein
- 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.
- 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
- 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