Clinical Research Coordinator/Study Nurse

Responsibilities

• Coordinate clinical research studies and maintain a safe study environment according to health and safety guidelines under the direction of the Principal Investigator
• Ensure patient well-being and address patient concerns while maintaining the highest quality of care
• Support staff with administrative tasks and provide direct patient care
• Maintain study protocols, Case Report Forms (CRFs), Electronic Data Capture (EDC) systems, and other essential study documentation
• Plan and coordinate logistical activities for study procedures in accordance with the protocol
• Perform clinical preparations, including labeling sample tubes, inventory management, and equipment setup
• Manage data entry, monitor data quality, and resolve queries
• Support patient recruitment, screening, and enrollment processes
• Collect and report clinical data and findings, including adverse events and serious adverse events (SAEs)
• Coordinate with study monitors to resolve issues and answer queries effectively

Requirements

• At least two years of relevant experience, or an equivalent combination of medical training and experience
• Strong knowledge of clinical trials, protocols, informed consent processes, and study plans
• Proficiency in MS Windows and Office applications (Excel, Word, Outlook, Access)
• Excellent interpersonal skills with the ability to build and maintain effective working relationships
• Very good German language skills (written and spoken)

About the Company

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.