Job Requirements:

• Minimum of Bachelor in Pharmacy or any science-related field
• Minimum 2 years of experience as a CRA
• Knowledge of GCP and clinical Trial regulations in Kuwait
• Fluency in Arabic and English

Job Description:

• Participate in the investigator recruitment process: performs initial qualification visits of potential investigators.
• Evaluate the capability of the site to successfully manage and conduct the clinical study, both clinically and technically
• Support site staff by providing the needed documents for the submission packages as per local regulations
• Ensure having all local approvals on study-specific documents before the site is initiated
• Perform all site visits from selection to close-out
• Train site staff on all clinical trial procedures and documents
• Train site staff on the EDC system and verifies site computer system
• Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits
• Perform a validation of source documentation as required by Sponsor and works with the site to resolve queries
• Prepare monitoring reports and letters in a timely manner using approved company /Sponsor forms and reports
• Document accountability, stability and storage conditions of clinical trial materials as required by Sponsor 
• Serve as the primary contact between the Sponsor and the site
• Ensure timely transmission of clinical data with the study site and technical reporting
• Assist with final data review and query resolution through database lock

Interested candidates can send their CVs to mdakhloul@phoenix-cr.com