Clinical Research Associate II
Remote
Job Summary
Monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations. Coordinate all necessary activities for study setup and monitoring, including identifying investigators, preparing regulatory submissions, and conducting pre-study and initiation visits. Identify potential study risks and propose mitigation solutions while maintaining quality and outcomes. This remote-based role in Hungary requires domestic travel including overnight stays, with a commitment of approximately 50-60% travel. Fluency in English and Hungarian is required, with oncology monitoring experience preferred.
Required Qualifications
- Life science degree and / or equivalent experience
- 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies
- Site management or equivalent experience in clinical research
- Availability for domestic travel including overnight stays, as required
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- Fluency in English and Hungarian
- Excellent communication and organizational skills
- A team player
- Evidence of a client focused approach
Desired Qualifications
- oncology monitoring experience will be a plus
- Study start up activities experience
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