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Experienced Clinical Research Associate

1+ years
$25,000 – $35,000 USD 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

Experienced Clinical Research Associate
Location: Georgia (Remote/Home-Based)

Job Description:
Medpace is expanding its presence in Georgia and is actively seeking experienced, home-based Clinical Research Associates (CRAs) to join its Clinical Monitoring team. This full-time, permanent role is a unique opportunity to contribute to building a local team and supporting clinical trials from start to finish. If you have prior independent monitoring experience and are looking for an exciting role with growth potential, Medpace offers a dynamic platform to grow your career in global drug development.

Key Responsibilities:

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

  • Perform source document verification, Case Report Form (CRF) review, and ensure data integrity.

  • Review and manage regulatory documentation as per ICH-GCP and local guidelines.

  • Oversee study drug inventory and ensure drug accountability at the site level.

  • Handle adverse event (AE) and serious adverse event (SAE) reporting and follow-ups.

  • Evaluate and support patient recruitment and retention strategies.

Qualifications:

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

  • At least 1 year of independent CRA monitoring experience.

  • Strong understanding of medical terminology, clinical patient care, and drug therapy.

  • Familiarity with clinical research methodologies, ICH GCP, and local regulatory requirements.

  • Proficiency in English and Georgian (oral and written).

  • High attention to detail and strong communication skills.

  • Must hold a valid driver’s license and be based in Georgia.

  • Applications must be submitted in English.

Why Join Medpace?

  • Opportunity to join a newly established local entity and shape its growth.

  • Competitive salary and benefits package.

  • Flexible remote work environment with structured support and training.

  • Defined career advancement paths and global exposure.

  • Access to a range of wellness and professional development initiatives.

About Medpace:
Medpace is a global full-service CRO, supporting Phase I–IV clinical trials for biotechnology, pharmaceutical, and medical device companies. With operations across 40+ countries and over 5,000 employees, Medpace delivers high-quality research services grounded in scientific and regulatory expertise across major therapeutic areas.

Awards & Recognition:

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

  • Winner of CRO Leadership Awards for quality, reliability, and performance excellence

Estimated Salary: $25,000 – $35,000 USD annually (based on Georgian market standards and experience level)