أحدث معلومات الوظائف من IQVIA LLC لمنصب Site Coordinator. If the Site Coordinator الشاغرة في Riyadh تتوافق مع مؤهلاتك، يرجى تقديم أحدث طلب أو سيرة ذاتية مباشرة من خلال بوابة وظائف Jobkos المحدثة.
يرجى ملاحظة أن التقديم على وظيفة قد لا يكون سهلاً دائماً، حيث يجب على المرشحين الجدد استيفاء مؤهلات ومتطلبات معينة تحددها الشركة. نأمل أن تكون الفرصة المهنية في IQVIA LLC لمنصب Site Coordinator أدناه تتوافق مع مؤهلاتك.
Site Coordinator page is loaded## Site Coordinatorالموقعs: Riyadh, المملكة العربية السعوديةtime type: Full timeنُشر في on: نُشر في Todaytime left to apply: End Date: January 9, 2026 (8 days left to apply)job requisition id: R1521758Job OverviewPerform 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 الشركة, الدولة, state, and/or other regulatory bodiesIQVIA 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. #J-18808-Ljbffr
معلومات الوظيفة:
الشركة: IQVIA LLC
المنصب: Site Coordinator
مكان العمل: Riyadh
الدولة: SA
كيفية تقديم الطلب:
بعد قراءة وفهم المعايير ومتطلبات الحد الأدنى من المؤهلات الموضحة في معلومات الوظيفة Site Coordinator at the office Riyadh أعلاه، أكمل فوراً ملفات طلب الوظيفة مثل خطاب التقديم، السيرة الذاتية، نسخة من الشهادة الجامعية، كشف الدرجات، والملاحق الأخرى كما هو موضح أعلاه. أرسلها عبر رابط الصفحة التالية أدناه.
انتهت صلاحية هذا الإعلان الوظيفي (منذ أكثر من 30 يوماً).
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