Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Experienced Clinical Research Associate

Medpace
Medpace
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)