Sponsor-Dedicated Sr. Clinical Research Associate

Clinical Consultation Club Corporation (4

Cs) is a clinical research consulting firm specializing in supporting biotechnology, pharmaceutical, medical device, contract research organizations (CROs), and site management organizations (SMOs). With a strong foundation in clinical development, project management, and medical monitoring, 4

Cs ensures precision and quality in every aspect of clinical trials. Their services include clinical monitoring, protocol execution, site engagement, and risk-based operational leadership to drive successful study delivery. Focused on practical, patient-centered solutions, 4

Cs is dedicated to meeting global regulatory standards and ensuring trial efficiency. Their mission is to enhance clinical research through collaborative partnerships and operational excellence.

As 4

Cs is planning to expand to the Middle East with two offices, one in Cairo, Egypt, and the other in Riyadh, KSA, we are at the stage of collecting resumes in preparation to hire two Sponsor‑Dedicated Senior Clinical Research Associates, one in each location. These two roles are hybrid, contract roles that involve monitoring clinical trial processes at investigative sites to ensure compliance with protocols, regulatory guidelines, and quality standards.

Responsibilities include site management, data review, documentation of findings, relationship‑building with site staff, risk assessment, adherence to timelines, and resolution of potential site‑related challenges. This role requires collaboration with sponsor teams and investigators to drive the success of clinical studies.

• Citizen or hold a valid transferable Iqama.
• Proficiency in clinical monitoring, site management, and regulatory compliance
• Experience in protocol execution, data review, and managing trial documentation
• Strong interpersonal and communication skills for collaborating with sponsor teams and site personnel
• Ability to perform risk assessments and ensure adherence to global regulatory and quality standards
• Highly organized, detail‑oriented, and capable of managing multiple priorities effectively
• Bachelor's degree or equivalent in a relevant scientific or healthcare field
• Certifications such as CCRP or CCRA are preferred
• Knowledge of ICH‑GCP guidelines and prior experience with clinical trials are highly desirable.
• English proficiency is required, and you must pass the IT Proficiency Assessment test.