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Experienced Clinical Research Associate

0-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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 (CRA)

Location: Estonia
Functional Area: Clinical Research Associate
Job ID: 10605
Employment Type: Full-time
Work Arrangement: Home-based


Job Summary:

Medpace is seeking Experienced Clinical Research Associates to join the Clinical Monitoring team in Estonia. This role is instrumental in supporting the growth of our new entity in Estonia and contributing to critical tasks and projects that drive the success of our clinical operations.

This position offers the opportunity to be involved in every stage of the drug development process, providing unmatched support to our clients. It is ideal for candidates with a health-related background who enjoy extensive travel and direct involvement in clinical trials.


Key Responsibilities:

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites.

  • Perform source document verification and case report form (CRF) review.

  • Review regulatory documents to ensure compliance.

  • Conduct study drug inventory management.

  • Perform adverse event (AE) and serious adverse event (SAE) reporting and follow-up.

  • Assess patient recruitment and retention at study sites.


Qualifications:

  • Education: Minimum Bachelor of Science in a health-related field, MD, or equivalent.

  • Experience: Minimum 1 year of independent CRA monitoring experience.

  • Knowledge & Skills:

    • Broad knowledge of medical terminology and clinical patient management.

    • Basic understanding of drug therapy techniques and clinical research methodologies.

    • Comprehensive knowledge of Local Regulations and ICH GCP.

    • Excellent oral and written communication skills.

    • Fluency in Estonian and English.

    • High attention to detail.

    • Must hold a valid driver’s license.


Medpace Overview:

Medpace is a full-service Clinical Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries. The company leverages local regulatory and therapeutic expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective areas.


Why Medpace:

  • Flexible work environment.

  • Competitive compensation and benefits package.

  • Paid time off and structured career growth opportunities.

  • Company-sponsored employee appreciation events.

  • Employee health and wellness initiatives.

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

  • Multiple CRO Leadership Awards from Life Science Leader magazine.