Employer Industry: Clinical Research Organization (CRO)

Why consider this job opportunity:
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives

What to Expect (Job Responsibilities):
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites
- Perform source document verification and case report form review
- Perform regulatory document review
- Conduct study drug inventory
- Perform adverse event and serious adverse event reporting and follow-up; assess patient recruitment and retention

What is Required (Qualifications):
- Minimum a Bachelor of Science in a health-related field, MD, or equivalent
- Minimum of 1 year independent CRA monitoring experience
- Broad knowledge 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

How to Stand Out (Preferred Qualifications):
- Fluency in Georgian and English
- Excellent oral and written communication skills
- Great attention to detail
- Must hold a valid driver’s license

#ClinicalResearch #HealthcareCareers #CareerGrowth #FlexibleWork #CRO

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