Clinical Research Associate

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profile Job Location:

Doha - Qatar

profile Monthly Salary: Not Disclosed
Posted on: 4 hours ago
Vacancies: 1 Vacancy

Job Summary

J

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

JClinical Research Monitor (CRM)Key Requirements (Must-Have):Fluency in spoken and written Arabic (Mandatory)Fluency in EnglishKey Responsibilities:Ensure compliance with approved protocols GCP ICH guidelines and regulatory requirements.Monitor study conduct to ensure participant safety and data int...
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