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Clinical Research Associate

1-2 years
Not Disclosed
10 Dec. 6, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences/ MD 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

Clinical Research Associate
Location: Georgia (Home-based)
Job ID: 9910

Job Summary:
Medpace is seeking full-time, home-based Clinical Research Associates (CRAs) to join our Clinical Monitoring team in Georgia. This is a new, permanent role, and as part of building our team in Georgia, the recruitment process may be extended, and some benefits may be confirmed but not yet in place based on candidates' preferred start date.

As a CRA at Medpace, you will play an instrumental role in the growth of the team and contribute to the success of clinical trials. You will have the opportunity to be involved in every stage of the drug development process and provide critical support to our clients. Our CRAs come from diverse medical and healthcare backgrounds, including Registered Nurses, Dieticians, Pharmacists, and Science Graduates. An extensive training program is provided to ensure success in the role.

Responsibilities:

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites.
  • Perform source document verification and case report form review.
  • Review regulatory documents.
  • Manage study drug inventory.
  • Report adverse events (AEs) and serious adverse events (SAEs), and follow-up as needed.
  • Monitor patient recruitment and retention.

Qualifications:

  • Bachelor’s degree in a health-related field (MD or equivalent preferred).
  • Minimum of 1 year of independent CRA monitoring experience.
  • Strong 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 in Georgian and English.
  • High attention to detail.
  • Valid driver’s license.

Medpace Overview:
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. Our mission is to accelerate the global development of safe and effective medical therapeutics. We leverage local regulatory and therapeutic expertise across all major therapeutic areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective.

Why Medpace?

  • Flexible work environment
  • Competitive compensation and benefits package
  • 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)
  • Awarded for excellence in the CRO industry by Life Science Leader magazine.

Join Medpace today and make a lasting impact on global health.