Clinical Research Associate

3 weeks ago


Riyadh, Saudi Arabia Celero - Providing optimal returns to innovativebiotechs Full time
  • Assists in the preparation andsubmission of clinical trial documents for review of ethicscommittees.
  • Conducts identification,evaluation, qualification, initiation, monitoring and visits ofinvestigators and sites (including close-outvisits).
  • Checks implementation of companystandard operational procedures (SOPs), sponsor procedures, ICH/GCPguidelines and regulatory requirements during clinical trials andensures the protection of study subjects by verifying that informedconsent procedures and protocol requirements are adheredto.
  • Assesses the site’s subjectrecruitment and retention success, verifies eligibility ofsubjects, and offers suggestions forimprovement.


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