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Experienced Clinical Research Associate

1-3 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Experienced Clinical Research Associate

Location: Georgia
Department: Clinical Research Associate
Job Type: Full-time, Home-Based


ABOUT MEDPACE

Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.

Headquartered in Cincinnati, Ohio, Medpace operates in 40+ countries with over 5,000 employees. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach, leveraging local regulatory and therapeutic expertise in key areas such as oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective research.


JOB SUMMARY

Medpace is expanding its clinical activities in Georgia and is seeking full-time, home-based Clinical Research Associates (CRAs) to join the Clinical Monitoring team.

This role will be instrumental in growing the team in Georgia and supporting key clinical research projects. The CRA will be involved in every stage of the drug development process and will have the opportunity to develop and advance their career in clinical research.

Note: This role is not U.S.-based and requires candidates to be located in Georgia.


KEY RESPONSIBILITIES

Site Management & Monitoring

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites.
  • Perform source document verification and case report form (CRF) review.
  • Conduct regulatory document review to ensure compliance.
  • Oversee study drug inventory and accountability.
  • Assess patient recruitment and retention and suggest improvements.

Safety & Compliance

  • Ensure adverse event (AE) and serious adverse event (SAE) reporting and follow-up.
  • Maintain compliance with Local Regulations, ICH GCP guidelines, and Medpace SOPs.
  • Ensure accuracy and completeness of clinical trial data.

QUALIFICATIONS & EXPERIENCE

Education:

  • Bachelor’s degree in a health-related field (e.g., Medicine, Pharmacy, Life Sciences) or MD or equivalent.

Experience:

  • Minimum 1 year of independent CRA monitoring experience.

Technical & Regulatory Knowledge:

  • Strong understanding of medical terminology and clinical patient management.
  • Basic knowledge of drug therapy techniques and clinical research methodologies.
  • Comprehensive knowledge of Local Regulations and ICH-GCP guidelines.

Soft Skills & Language Requirements:

  • Fluency in Georgian and English (oral and written).
  • Excellent communication and organizational skills.
  • Strong attention to detail and time management skills.
  • Must hold a valid driver’s license for site visits.

Note: Applications should be submitted in English.


COMPENSATION & BENEFITS

Salary & Benefits:

  • Competitive compensation based on experience.
  • Flexible work environment (home-based).
  • Comprehensive benefits package.

Perks & Growth Opportunities:

  • Structured career paths with opportunities for professional growth.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness initiatives.
  • Competitive PTO package.

AWARDS & RECOGNITION

  • Forbes: America's Most Successful Midsize Companies (2021, 2022, 2023, 2024).
  • CRO Leadership AwardsLife Science Leader Magazine (Expertise, Quality, Capabilities, Reliability, Compatibility).

HOW TO APPLY

If you are an experienced Clinical Research Associate seeking an exciting opportunity to contribute to clinical trials in Georgia, apply now to join Medpace’s growing team!