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Experienced Clinical Research Associate

1+ years
€40,000 – €55,000 annually
10 July 30, 2025
Job Description
Job Type: Full Time Education: MD/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

Experienced Clinical Research Associate
Location: Croatia
Job Role: Clinical Research Associate
Job ID: 11140

Job Summary:
Medpace is expanding its European operations and is currently seeking a full-time, home-based Clinical Research Associate (CRA) to join its Clinical Monitoring team in Croatia. This is a permanent role within a newly established entity in Croatia, and the recruitment timeline or benefits package may vary based on the candidate’s start date.

This position is crucial to establishing a strong foundation for Medpace's clinical research operations in Croatia. It offers a dynamic and fulfilling opportunity for individuals with medical or health-related education and a passion for contributing to the clinical trials process.

Key Responsibilities:

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites as per the protocol.

  • Communicate with site staff including coordinators, investigators, and other medical personnel.

  • Ensure investigator and site qualifications, including verification of training, equipment, and facilities.

  • Review and verify medical records and source documents against case report forms (CRFs).

  • Ensure good documentation practices and address any protocol deviations as per SOPs and regulatory requirements.

  • Verify subject eligibility and ensure proper subject enrollment practices.

  • Review regulatory documents and perform investigational product accountability.

  • Monitor and report adverse/serious adverse events, concomitant medications, and related illnesses.

  • Assess and support site recruitment and retention strategies.

  • Complete detailed monitoring visit reports and follow-up letters summarizing key findings.

Qualifications:

  • Minimum of a Bachelor’s degree in a health-related field, MD, or equivalent.

  • At least 1 year of independent CRA monitoring experience.

  • Broad knowledge of medical terminology and patient management.

  • Basic understanding of drug therapies and clinical research methodologies.

  • Strong understanding of local regulations and ICH GCP guidelines.

  • Excellent written and verbal communication skills in Croatian and English.

  • Exceptional attention to detail and organizational skills.

  • Valid driver’s license required.

  • Applicants are requested to submit applications in English.

About Medpace:
Medpace is a global, full-service clinical contract research organization (CRO) headquartered in Cincinnati, Ohio. With over 5,000 employees across 40+ countries, we offer comprehensive services for Phase I-IV clinical trials. Our therapeutic expertise spans oncology, cardiology, CNS, endocrinology, infectious diseases, and more.

Why Join Medpace?

  • Flexible work environment

  • Competitive salary and benefits

  • Generous paid time off (PTO)

  • Structured career development programs

  • Health and wellness initiatives

  • Frequent employee appreciation events

Awards & Recognition:

  • Forbes: America’s Most Successful Midsize Companies (2021–2024)

  • CRO Leadership Awards: Recognized for expertise, reliability, quality, and compatibility

Next Steps:
Candidates will be contacted by a Medpace representative if selected for further evaluation.

Estimated Salary: €40,000 – €55,000 annually (based on role and experience in Croatia)