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Senior Clinical Research Associate Contractor

3+ years
€55,000 – €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: 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