Clinical Research Associate
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Job Summary
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Clinical Research Monitor (CRM)
Key Requirements (Must-Have):
Fluency in spoken and written Arabic (Mandatory)
Fluency in English
Key Responsibilities:
Ensure compliance with approved protocols GCP ICH guidelines and regulatory requirements.
Monitor study conduct to ensure participant safety and data integrity.
Review informed consent source documents CRFs ISF and adverse event reporting.
Conduct monitoring visits prepare reports and follow up on CAPA actions.
Coordinate closely with Principal Investigators research teams and IRB.
Manage multiple studies while meeting quality and timeline expectations.
Qualifications:
Bachelor’s degree in Health/Biomedical Sciences (Master’s preferred).
5 years’ experience in clinical research monitoring in an FDA/EMA-regulated environment.
Strong knowledge of GCP and clinical research regulations.
OB SUMMARY
