Site Coordinator

Site Coordinator page is loaded## Site Coordinator locations:
Riyadh, Saudi Arabiatime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
January 9, 2026 (8 days left to apply) job requisition :
R1521758

Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning.
Essential Functions
• Provide clinical research support to investigators to prepare for and execute assigned research studies, including:  
• Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data  
• Attend all relevant study meetings  
• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research  
• Recruit and screen patients for clinical trials and maintain subject screening logs  
• Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits  
• Design and maintain source documentation based on protocol requirements  
• Schedule and execute study visits and perform study procedures  
• Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness  
• Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics  
• Monitor subject safety and report adverse reactions to appropriate medical personnel  
• Correspond with research subjects and troubleshoot study-related questions or issues  
• Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards  
• Assist with study data quality checking and query resolution.  
• Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.  
• Record, report and interpret study findings appropriately to develop a study-specific database.  
• Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.  
• Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.  
• Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.  
• Assist research site with coverage planning related to staffing and scheduling for research projects.
Qualifications
• Bachelor's Degree  
• 3 years’ relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training and experience
• 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 Word  
• Excellent interpersonal skills  
• Ability to pay close attention to detail  
• Ability to establish and maintain effective working relationships with coworkers, managers and clients  
• Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies

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