Clinical Research Associate

Management Solutions International MSI

موقع الوظيفة:

الدوحة - قطر

الراتب شهرياً: لم يكشف

تاريخ النشر: نُشرت قبل 9 ساعة

عدد الوظائف الشاغرة: 1 عدد الوظائف الشاغرة

سجل للتقديم

ملخص الوظيفة

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...