Clinical Research Coordinator

IQVIA LLC; Riyadh; On-site; SAR 150,000 - 200,000; Full time

Job summary

A global healthcare services company in Riyadh is looking for a Clinical Research Coordinator. This role involves coordinating clinical studies, ensuring the well-being of subjects, and managing study protocols and documentation. The ideal candidate will have a Bachelor's degree and 2-3 years of onsite experience, alongside knowledge of clinical trials and Good Clinical Practices. Responsibilities include oversight of procedures, data quality checking, and volunteer recruitment. An exciting opportunity to join a team dedicated to improving patient outcomes.

Qualifications

• 2-3 years of actual onsite experience in clinical research.
• Knowledge of clinical trials and Good Clinical Practices (GCP).
• Skill in performing clinical procedures like phlebotomy.

Responsibilities

• Coordinate clinical research studies and maintain safety.
• Safeguard subjects' well-being and address concerns.
• Assist in study enrollment and perform complex clinical procedures.

Skills

Clinical procedures execution

Data quality checking

Volunteer recruitment

MS Windows and Office

Education

Bachelor's Degree

Job description

Clinical Research Coordinator - (Onsite) page is loaded## Clinical Research Coordinator - (Onsite)locations: Riyadh, Saudi Arabiatime type: Full timeposted on: Posted Todaytime left to apply: End Date: January 27, 2026 (12 days left to apply)job requisition id: R1521183## Role Responsibilities:* ## Coordinate clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator* ## Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns while ensuring the highest quality-of-care practices* ## Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents* ## Plan and coordinate logistical activity for study procedures according to the study protocol* ## Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues* ## Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness* ## Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol* ## Correct custody of study drug according to site standard operating procedures* ## Perform a variety of complex clinical procedures on subjects including but not limited to vital signs, phlebotomy, etc.* ## Collect, record, and report clinical data and findings appropriately in CRFs while collaborating with study investigator about study-related adverse events and serious adverse events according to the study protocol.## ## Qualifications## * ## Bachelor's Degree* ## Actual onsite experience (2-3 years)* ## Working knowledge of clinical trials* ## Working knowledge of the principles of Good Clinical Practices (GCP)* ## In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules* ## Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing* ## Good skill in using MS Windows and Office applications such as Access, Outlook and WordIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.