Experienced Clinical Research Associate
GE
International Careers
Req #: 10606
Type: Full-Time
|
|
|||||||||||
|
||||||||||||
Overview: Medpace is a full-service clinical contract research organization (CRO). We provide 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 through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. 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; and * Assess patient recruitment and retention Qualifications: * Minimum a Bachelor of science in health-related field, MD or equivalent * Minimum of 1 year independent CRA monitoring * 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 * Excellent oral and written communication skills * Fluency in Georgian and English * Great attention to detail * Must hold a valid driver's license * We kindly ask to submit applications in English
Share this job:
