Clinical Research Associate Full Time

Job open for applicants based in Beirut (Lebanon), Dubai (United Arab Emirates), and Riyadh (Kingdom of Saudi Arabia).

About the Role 

This is a junior clinical research position within CCHO’s Evidence Generation team. You will work under the direction of the Real-World Evidence (RWE) Manager, providing operational support to clinical research projects. As a Clinical Research Associate, you will help execute and monitor clinical trials to ensure they are conducted in compliance with the study protocol, Good Clinical Practice (GCP), regulatory requirements, and sponsor SOPs. You will act as the primary liaison between the sponsor/CRO and investigational sites — with direct mentorship and clear room to grow. 

What You’ll Do 

Protocol & Clinical Trial Monitoring 

• Draft assigned proposal/protocol sections under supervision and assist with amendments and version control 
• Support site qualification, initiation, routine monitoring, and close-out visits (on-site and/or remote) 
• Verify informed consent processes and documentation; ensure subject safety, rights, and well-being 
• Perform source data verification (SDV) and data review; identify and report protocol deviations 

Regulatory & Compliance 

• Ensure compliance with ICH-GCP, local regulations, and sponsor SOPs 
• Review and maintain essential trial documentation (TMF/ISF) 
• Prepare IRB packages for submission to institutions/regulatory authorities as applicable 
• Maintain study documentation for compliance purposes as well as for upcoming inspections, and audits 
• Ensure proper reporting of adverse events (AEs) and serious adverse events (SAEs) 

Platform & System Testing 

• Conduct dry runs and user acceptance testing (UAT) of data capture platforms 
• Document test results and report issues to the senior team 
• Support system validation activities 

Literature Review & Data Extraction 

• Conduct targeted literature searches using PubMed, Embase, and Cochrane 
• Extract and summarize relevant data from published sources 
• Maintain reference libraries and citation records 

Study Coordination, Data & Reporting 

• Update and maintain study-specific site trackers, and study logs (meeting minutes, slide decks, action plan tables…) under supervision 
• Conduct data collection activities under supervision; review EDC data and manage queries 
• Conduct qualitative interviews (if applicable) under supervision 
• Prepare monitoring visit reports and follow-up letters 
• Maintain study documentation, training records, and audit trail documentation 

What We’re Looking For 

• Bachelor’s degree in Life Sciences, Public Health, Pharmacy, Nursing, or a related scientific field; Master’s degree is an asset 
• 0–2 years in clinical research, healthcare, or a related field — fresh graduates are considered for this entry-level position 
• Basic understanding of clinical research terminology, study designs, and GCP principles 
• Familiarity with IRB submissions, literature review and medical writing 
• Attention to detail for accurate documentation and clear written and verbal communication skills 
• Basic awareness of pharmacovigilance and adverse event reporting is an advantage 
• Familiarity with EDC systems and literature databases (PubMed, Embase, Cochrane) is a plus 
• Fluency in English and Arabic language preferred