Clinical Research Coordinator: Trials, Data & Compliance

King Faisal Specialist Hospital & Research Centre

Saudi Arabia

On-site

SAR 60,000 - 100,000

Full time

14 days+

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Job summary

King Faisal Specialist Hospital & Research Centre is seeking a clinical research professional to design and execute studies and ensure protocol compliance. The role supports the ORA team and coordinates daily activities, data collection, and reporting.

Requirements include a Master’s or Bachelor’s in health sciences, nursing, or pharmacy; Saudi national status; and preferred NIH training or accredited online courses. Prior experience in clinical research is valued.

Qualifications

  • Master's or Bachelor's degree in health science–related field.
  • 2 years with Master's or 4 years with Bachelor's.
  • Saudi national only.
  • Clinical Research Professional course or accredited online course preferred.
  • NIH training in Protecting Human Research Participants preferred.

Responsibilities

  • Assist in designing and executing clinical research projects and ensure protocol compliance.
  • Coordinate daily clinical research activities and data collection.
  • Perform data entry, statistics, and interpretation with principal investigators.
  • Monitor protocols and report progress per ORA procedures.
  • Recruit patients, obtain informed consent, collect samples, record vital signs, and manage forms.
  • Prepare technical reports and ensure timely completion of tasks.

Skills

Clinical research
Data collection
Protocol compliance
Study coordination

Education

Health science degree

Tools

NIH training

Job description

King Faisal Specialist Hospital & Research Centre is seeking a clinical research professional to design and execute studies and ensure protocol compliance. The role supports the ORA team and coordinates daily activities, data collection, and reporting.

Requirements include a Master’s or Bachelor’s in health sciences, nursing, or pharmacy; Saudi national status; and preferred NIH training or accredited online courses. Prior experience in clinical research is valued.

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