Instagram
youtube
Facebook

Senior Clinical Research Associate, Contractor, Hungary

3+ years
HUF 13,000,000 – 16,000,000 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: Hungary
Job Type: Contract | Category: Clinical Operations
Estimated Salary: HUF 13,000,000 – 16,000,000 annually (based on Hungarian clinical research industry standards)


About Biorasi:
Biorasi is an award-winning, full-service Clinical Research Organization (CRO) known for its innovation, agility, and commitment to improving global health. We provide an empowering work culture that supports professional growth and work-life balance while helping to bring cutting-edge therapies to market.


Position Overview:
As a Senior Clinical Research Associate (CRA) Contractor in Hungary, you will be responsible for overseeing and executing all phases of clinical trial site management. This fully remote role requires extensive site-facing experience, coordination with global teams, and regulatory compliance expertise.


Key Responsibilities:

  • Conduct all types of site visits: selection, initiation, interim monitoring, and close-out

  • Prepare visit reports and follow-up letters after each site visit

  • Monitor the overall progress of assigned studies: IRB approvals, recruitment, data collection, and query resolution

  • Coordinate logistics of study materials, investigational products, and site documentation

  • Participate in and support Investigator Meetings and protocol training

  • Ensure compliance with study protocols, ICH-GCP guidelines, and subject safety documentation

  • Collect, review, and maintain essential regulatory documents in eTMF

  • Establish and maintain strong communication lines with study sites

  • Evaluate site performance and adherence to applicable regulations

  • Support quality assurance planning and resolve audit findings as needed

  • Assist Clinical Trial Manager in operational oversight, team mentoring, and CRA/CTA support

  • May participate in document review (protocols, eCRFs, study manuals) and site staff training

  • Attend regular team meetings and teleconferences to report progress and performance


Candidate Requirements:

  • Bachelor’s degree in biomedical sciences or a related discipline

  • Fluency in English and the Hungarian language

  • Minimum 3 years of monitoring or clinical research experience (CRA or CRC roles)

  • Strong understanding of medical terminology and the clinical monitoring process

  • Familiarity with ICH-GCP and global regulatory requirements

  • Proficient with Microsoft Office Suite (Word, Excel, PowerPoint)

  • Willingness to travel up to 70% for site visits and meetings

  • Excellent leadership, planning, organizational, and communication skills


Why Join Biorasi?

  • Work in a dynamic, fast-growing CRO with global reach

  • Join a culture of innovation, inclusion, and collaboration

  • Competitive compensation and flexible work environment

  • Impactful role that contributes to life-changing research


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