Senior Clinical Research Associate Contractor
Location: Czech Republic
Job Type: Full-time | Remote Type: Onsite/Field-Based
Category: Clinical Operations
Estimated Salary: €55,000 – €75,000 annually (based on industry standards in the EU region)
About Biorasi:
At Biorasi, we are reshaping the clinical research landscape with an innovative and collaborative approach. As an award-winning, full-service clinical research organization (CRO), we are rapidly growing and seeking passionate professionals who thrive in dynamic environments. Join us to drive new therapies from research to reality.
Role Summary:
As a Senior Clinical Research Associate (CRA) Contractor, you will be pivotal in executing and monitoring clinical trials from start to finish. Your work will ensure the quality and integrity of study site operations, adherence to regulatory standards, and the successful delivery of project milestones.
Key Responsibilities:
Conduct all types of site visits: selection, initiation, interim, and close-out
Prepare visit reports and follow-up letters
Track and support regulatory/IRB submissions, site recruitment, CRF completion, and query resolution
Provide regular project updates to the management team
Coordinate delivery and return of investigational products and study materials
Perform investigational product accountability and compliance verification
Participate in and help organize Investigator Meetings
Review study documents to ensure compliance and escalate protocol deviations
Collect essential site documents for eTMF filing
Train site staff on protocol and study procedures
Monitor site performance and ensure GCP and protocol adherence
Support audits and assist in resolving audit findings
Collaborate with CTMs to manage resources and site performance
Assist in preparing study documents including protocols, CRFs, and manuals
May mentor junior associates and CRAs
Participate in team meetings and provide feedback on study progress
Other responsibilities as assigned
Candidate Profile:
Bachelor’s degree in biomedical sciences or a related field
Fluent in English and local business language
Minimum 3 years of clinical monitoring experience (more preferred)
Solid understanding of medical terminology and GCP standards
Ability to travel up to 70% based on project needs
Strong planning, leadership, and communication skills
Proficiency in Microsoft Office (Word, Excel, PowerPoint)
Why Join Biorasi?
Contribute to a dynamic and fast-growing global CRO
Flexible, supportive, and growth-oriented work culture
Opportunity to work on meaningful projects impacting global health
Competitive compensation for contractors and potential future collaborations
To Apply:
Submit your application directly through biorasi.com or email your resume to: careers@biorasi.com
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