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Senior Clinical Research Associate, Contractor, Czech Republic

3+ years
€52,000 – €75,000 annually
10 July 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Research Associate, Contractor
Location: Czech Republic
Job Type: Contract | Category: Clinical Operations
Estimated Salary: €52,000 – €75,000 annually (based on Czech Republic clinical contractor benchmarks)


About Biorasi:
Biorasi is a full-service, award-winning Clinical Research Organization (CRO) built around innovation, flexibility, and an unshakable focus on customer satisfaction. As we expand globally, we seek clinical professionals ready to support life-changing therapies and thrive in a fast-paced, rewarding environment.


Role Summary:
As a Senior Clinical Research Associate (CRA) Contractor, you will manage essential monitoring activities to ensure smooth site operations and compliance across all stages of the clinical trial lifecycle. This role supports local sites in the Czech Republic and may require frequent travel.


Core Responsibilities:

  • Conduct Site Visits: selection, initiation, monitoring, and close-out

  • Prepare reports and follow-up letters from each visit

  • Oversee study progress including IRB approvals, patient recruitment, CRF submissions, and query resolutions

  • Coordinate shipment and logistics for investigational products and study supplies

  • Attend and assist with Investigator Meetings

  • Review documentation for protocol, ICH GCP, and safety compliance

  • Ensure proper eTMF documentation and version control

  • Deliver protocol training and maintain consistent communication with study sites

  • Provide input to Clinical Trial Managers on site performance and study metrics

  • Address audit findings and contribute to quality improvement processes

  • Participate in team meetings, and contribute to project performance feedback

  • Mentor junior CRAs and support cross-functional collaborations


Ideal Candidate Profile:

  • Bachelor's Degree in biomedical sciences or related field

  • Fluent in English and local Czech language

  • Minimum 3 years of CRA experience (more preferred)

  • Strong understanding of ICH-GCP guidelines and local regulatory environment

  • Excellent written and verbal communication skills

  • Confident with MS Office tools (Word, Excel, PowerPoint)

  • Willingness to travel up to 70% as needed

  • Skilled in problem-solving, project coordination, and cross-functional communication


Why Biorasi?

  • Be part of a growing global CRO

  • Contribute to meaningful clinical advancements

  • Enjoy flexible work-life balance and a collaborative culture

  • Engage in impactful, global studies across therapeutic areas


How to Apply:
Submit your application via
biorasi.com or email your resume to careers@biorasi.com