Instagram
youtube
Facebook

Senior Clinical Research Associate, Contractor, Bosnia And Herzegovina

3+ years
€50,000 – €72,000 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: Bosnia and Herzegovina
Job Type: Contract | Category: Clinical Operations
Estimated Salary: €50,000 – €72,000 annually (based on regional CRO contractor rates)


About Biorasi:
At Biorasi, we champion innovation, collaboration, and growth in clinical research. As an award-winning, full-service CRO, we are actively expanding our global footprint. We seek high-performing professionals ready to contribute to life-changing clinical trials that bring new therapies to patients worldwide.


Role Overview:
As a Senior Clinical Research Associate (CRA) Contractor based in Bosnia and Herzegovina, you will play a critical role in managing and monitoring clinical trial activities, ensuring strict compliance with protocol, GCP, and regulatory guidelines.


Key Responsibilities:

  • Plan, schedule, and conduct all types of site visits: selection, initiation, monitoring, and close-out

  • Prepare reports and follow-up letters post-visit

  • Track regulatory submissions, recruitment status, CRF completion, and data query resolution

  • Manage investigational product and study supply inventory and logistics

  • Support Investigator Meetings and provide on-site training

  • Ensure proper documentation and eTMF filing compliance

  • Identify protocol deviations, review safety events, and escalate issues as needed

  • Maintain open communication channels with study sites to manage expectations and resolve challenges

  • Participate in audits and contribute to quality assurance planning

  • Assist the Clinical Trial Manager with resource allocation, site performance review, and documentation oversight

  • Mentor junior team members and contribute to overall study performance analysis


Candidate Profile:

  • Bachelor's degree in biomedical sciences or a related field

  • Fluent in English and the local language

  • Minimum 3 years of monitoring experience (CRA or CRC background preferred)

  • In-depth knowledge of clinical trial processes and medical terminology

  • Familiar with ICH-GCP guidelines and regional regulations

  • Strong written, verbal, planning, and project management skills

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

  • Ability to travel up to 70% depending on project requirements


Why Join Biorasi?

  • Fast-growing, globally recognized CRO with a strong commitment to quality

  • Opportunity to work on high-impact clinical studies

  • Supportive team culture that values innovation and diversity

  • Flexible, remote/field-based work structure


How to Apply:
Visit
biorasi.com to submit your application or email your CV to careers@biorasi.com