Senior CRA
On-site · Budapest, Budapest, Hungary
Job Summary
Senior Clinical Research Associate responsible for leading clinical trial monitoring tasks with a focus on quality and continuous improvement. Activities include monitoring sites to ensure adherence to study protocols, regulatory requirements, and GCP standards; conducting site visits to assess performance and resolve issues; collaborating with cross-functional teams to ensure timely data collection and reporting; providing training and guidance to site staff to maintain high standards of clinical trial conduct; and building strong relationships with site personnel and stakeholders to facilitate smooth trial operations. The role requires the ability to work independently, manage multiple sites/projects, travel approximately 60%, and ensure compliance throughout the trial lifecycle.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- Strong understanding of clinical trial processes and regulatory requirements
Desired Qualifications
- Senior Clinical Research Associate experience
- travel approximately 60%
- ability to lead on monitoring tasks
- training and mentoring site staff
- strong communication and stakeholder management skills
- proficiency with clinical trial software/tools
- data integrity and site management expertise
- ability to work independently
- cross-functional collaboration
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