Support study sites in coordinating Phase I–IV clinical research studies, ensuring compliance with study protocols, SOPs, GCP, and all applicable regulations. Contribute to participant safety, clinical procedures, study documentation, and operational workflow under the supervision of the Principal Investigator.
Main ActivitiesCoordinate daily study activities and support protocol execution.Maintain updated nursing and clinical research competencies.Ensure participant safety, act as a volunteer advocate, and maintain a safe environment.Perform clinical procedures (ECG, phlebotomy, vital signs, spirometry, cannulation, telemetry).Administer and manage study drug according to site SOPs.Review protocols, CRFs, study documents, and EDC systems.Prepare study materials, equipment, specimen labels, and logistical plans.Recruit, screen, and orient volunteers according to eligibility criteria.Collect, document, and report clinical data, including adverse events.Support data quality checks and query resolution.Participate in project meetings, monitoring visits, and daily huddles.Collaborate with monitors and ensure availability during monitoring activities.Troubleshoot study‑related issues and maintain protocol compliance.QualificationsNursing degree.Minimum 1 year of relevant experience or equivalent education and training.Strong knowledge of clinical trials and GCP principles.Proficiency in MS Windows and Office applications.Strong written and verbal communication skills in English.Excellent interpersonal, organizational, and problem‑solving abilities.High attention to detail and ability to work collaboratively with teams and clients.Active nursing license in the applicable state, country, or region.IQVIA 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 at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.