Join Resilience, a fast-growing and agile team at the forefront of digital, patient-centered clinical research. As a Clinical Research Associate (CRA), you will be directly involved in monitoring and managing ambitious multicenter studies across several therapeutic areas. You will play a key role in ensuring quality and compliance at every stage of clinical execution. This is a hands-on role offering strong exposure, autonomy, and the opportunity to grow within a collaborative and impact-driven environment.
Key missions
- Conduct site monitoring visits (initiation, routine, close-out) according to study plans.
- Ensure quality and completeness of clinical data and eCRFs, and manage protocol deviations.
- Serve as the key operational contact for investigator sites, and support visit planning and coordination.
Benefits
- Flexible working hours
- Open to full remote
- Reduction of working time (RTT)
- Cooptation bonus
- Stock purchase plan / Stock options
- Remote work allowance
- Team building
- Mental health benefits
- Full pay on 1st day of sick leave
- Professional development plan