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Experienced Clinical Research Associate

3+ years
€24,000 – €32,000 annually
9 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

Experienced Clinical Research Associate
Location: Serbia (Home-Based)

Job Description:
Medpace is expanding its operations in Serbia and is currently hiring full-time, home-based Clinical Research Associates (CRAs) to join the Clinical Monitoring team. This role offers a unique opportunity to be actively involved in the entire lifecycle of global clinical trials, contributing to pivotal research efforts. If you are experienced, detail-oriented, and passionate about clinical research, this is your chance to grow with a leading CRO.

Key Responsibilities:

  • Conduct qualification, initiation, monitoring, and closeout visits at clinical research sites.

  • Maintain close communication with investigators, site coordinators, and site staff.

  • Verify investigator qualifications, resources, and regulatory compliance.

  • Perform source data verification and ensure adherence to Good Clinical Practice (GCP).

  • Ensure accurate drug/device accountability and inventory tracking.

  • Validate subject eligibility and proper adverse event reporting.

  • Evaluate site recruitment performance and suggest strategies for improvement.

  • Document findings via monitoring reports and follow-up letters, including deviations and CAPA recommendations.

Qualifications:

  • Minimum Bachelor’s degree in Life Sciences or a Health-related field.

  • At least 3 years of prior CRA experience.

  • Familiarity with ICH-GCP, clinical documentation, ISF management, and regulatory submissions.

  • Proficiency in Microsoft Office and general computer literacy.

  • Fluent in English and Serbian (spoken and written).

  • Strong presentation, communication, and time management skills.

  • Willingness to travel 20–30% of the time.

  • Applications must be submitted in English.

Why Join Medpace?

  • Work from home with travel for site visits.

  • Competitive salary and benefits package tailored for the Serbian market.

  • Access to structured training, career development, and global exposure.

  • Recognized for leadership, reliability, and high-performance CRO services.

  • Culture that values passion, purpose, and people.

About Medpace:
Medpace is a global full-service CRO offering Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device clients. With a presence in 40+ countries and over 5,000 professionals, Medpace delivers a scientific, regulated, and patient-focused approach to clinical research.

Awards & Recognition:

  • Ranked by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)

  • Multiple CRO Leadership Awards for expertise, reliability, and capabilities

Estimated Salary: €24,000 – €32,000 annually (based on local CRA experience in Serbia)