Clinical Research Coordinator; CRC)

Pharma Knowl is a Saudi-based CRO and regulatory affairs service provider that supports pharmaceutical, biotechnology, and Med Tech companies

The Clinical Research Coordinator (CRC) is a full-time, on-site role based in Riyadh, Saudi Arabia. The CRC will coordinate day-to-day clinical trial activities, including participant screening, enrollment, and scheduling in alignment with approved study protocols. Responsibilities include organizing and documenting informed consent processes, maintaining accurate study records and source documents, and ensuring data is collected, entered, and managed according to GCP and SFDA regulatory standards.

The CRC will support investigators and monitors during site visits, prepare and update regulatory and ethics committee submissions, and assist with safety reporting and query resolution. The role also involves close collaboration with cross-functional teams, adherence to timelines, and continuous oversight of site compliance and quality.

• Minimum 1 year of clinical research experience.
• Experience in interventional clinical trials and direct patient interaction is preferred
• Bachelor’s degree in a medical or health-related field.
• Knowledge of ICH-GCP guidelines
• Good knowledge of EDC platforms and clinical data entry.
• Fair understanding of GCP and clinical trial procedures.
• Strong organizational and time-management skills, with the ability to manage multiple studies or tasks and meet deadlines.