Clinical Research Monitor

Job Opening: Clinical Research Monitor

Department: Human Research Subjects Protection Program

Location: Qatar

Key Responsibilities

• Monitor clinical research studies for compliance with GCP, protocols, and regulations
• Conduct monitoring visits and prepare detailed monitoring reports
• Review informed consent, CRFs, source data, adverse events, and protocol deviations
• Support research team training and site initiation visits
• Track, report, and escalate monitoring findings to HRPP Director and IRB

Qualifications & Requirements

• Bachelor’s degree in Biology, Health, or Biomedical Sciences
• 5+ years experience in clinical research monitoring or QA (FDA/EMA-regulated environment)
• Strong knowledge of ICH-GCP and regulatory requirements
• Fluency in English
• Proficiency in Microsoft Office and electronic systemsEnsure timely completion of monitoring activities

Job Type: Contract
Contract length: 3 months

Pay: QAR8,000.00 - QAR10,000.00 per month