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
$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)