Clinical Research Associate I/ Clinical Research Associate II
Related skills
clinical trials site monitoring regulatory submissions oncology sops📋 Description
- Monitor and own progress of clinical studies at investigative sites.
- Ensure studies conducted, recorded and reported per protocol and ICH-GCP.
- Coordinate site setup and monitoring (investigators, submissions, visits).
- Remote-based role with travel to sites; Paris area preferred.
- Focus on oncology and rare diseases; collaborative culture.
🎯 Requirements
- Life science degree or equivalent experience.
- 1+ year CRA experience in CRO or pharma.
- Experience managing oncology studies.
- Domestic travel incl. overnight stays; international travel may be required.
- Excellent communication and organizational skills.
- English plus local language proficiency where applicable.
- Study startup activities experience (preferred).
🎁 Benefits
- Remote-based position with travel to sites.
- Travel up to 50-60%.
- Influence and impact with direct line management support.
- Join a team focused on oncology and rare diseases.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Healthcare Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!