Freelance Senior Clinical Research Associate - Georgian Speaking - 0.5 Fte
ProPharma
Hybrid
Georgian and english speaking
Clinical monitoring
Gcp and regulatory requirements
ProPharma is seeking a Freelance Senior Clinical Research Associate (SCRA) who is fluent in both Georgian and English, with at least five years of experience in clinical research. The role involves clinical monitoring, site management, and ensuring compliance with regulatory standards, following a hybrid work model
Job Summary
The Senior Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites, ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, Good Clinical Practices (GCP) and other applicable regulatory requirements.
Main Responsibilities include conducting all types of monitoring visits, report writing, site personnel management and training, and reviewing source documents and case report forms for accuracy, completeness, and integrity of the data.
ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle, offering an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate partners’ most high-profile drug and device programs.
Matching Summary
Match Score: 85
ProPharma is seeking a Freelance Senior Clinical Research Associate (SCRA) who is fluent in both Georgian and English, with at least five years of experience in clinical research. The role involves clinical monitoring, site management, and ensuring compliance with regulatory standards, following a hybrid work model.
Skills & Requirements
Must-have
Georgian and English speaking
Clinical monitoring
GCP and regulatory requirements
Site initiation, interim, and close out visits
Monitoring report writing
Electronic data capture (EDC)
CTMS, IVRS, and eTMF experience
Nice-to-have
Excellent communication and interpersonal skills
Proactive planning and problem-solving
Attention to detail
Diversity, equity, and inclusion
Key Requirements
> 5 years of experience as a Clinical Research Associate
Bachelor's degree or equivalent combination of education and experience