Clinical Research Coordinator (CRC)

PharmaKnowl Consulting; Riyadh; On-site; SAR 90,000 - 150,000; Full time

Job summary

PharmaKnowl Consulting in Riyadh, Saudi Arabia, seeks a Clinical Research Coordinator (CRC) to manage day-to-day trial activities on-site. You will screen participants, enroll them, schedule visits, and coordinate informed consent documentation in line with approved protocols.

Responsibilities include maintaining accurate source documents, data entry per ICH-GCP and SFDA standards, supporting site visits, and preparing regulatory submissions.

Qualifications

• Bachelor’s degree in a medical or health-related field.
• Minimum 1 year of clinical research experience.
• 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.

Responsibilities

• Coordinate day-to-day clinical trial activities on-site in Riyadh.
• Screen participants, enroll them, and schedule visits per protocol.
• Organize and document informed consent processes and source documents.
• Ensure data is collected and managed per GCP and SFDA standards.
• Support investigators during site visits and regulatory submissions.
• Assist with safety reporting and data query resolution.
• Collaborate with cross-functional teams to meet timelines and quality standards.

Skills

Organizational skills

Time management

GCP knowledge

ICH-GCP guidelines

EDC platforms

Education

Bachelor’s degree in medical/health field

Tools

EDC platforms

Job description

PharmaKnowl is a Saudi-based CRO and regulatory affairs service provider that supports pharmaceutical, biotechnology, and MedTech companies

Role Description

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.

Qualifications

• 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.