Clinical Research Coordinator / Study Nurse (m/f/d) - Neuwied

Are you looking for a new opportunity or challenge in clinical research? Would you like to work for an industry-leading company?

IQVIA is currently looking for an ** Clinical Research Coordinator / Study Nurse (m/f/d)** to support the conduct of a clinical study at a center in Neuwied.

This position is available immediately, initially limited to 6 months. The scope is 24 hours per week.

Daily tasks include:

• Coordinating clinical research studies and maintaining a safe study environment according to health and safety guidelines under the direction and delegation of the Principal Investigator
• Ensuring the well-being of patients, addressing their concerns while ensuring the highest quality
• Caring for patients and supporting staff with administrative tasks
• Maintaining study protocols, case report forms (CRFs), electronic data capture systems (EDC), and other study documents up to date
• Planning and coordinating logistical activities for study procedures according to the study protocol
• Conducting clinical preparations for the study, including labeling sample collection tubes and containers, inventorying required materials, and setting up or troubleshooting equipment and/or the study
• Data entry, data quality review, and responding to queries
• Supporting patient enrollment in the study through recruitment, screening, and briefing according to the study protocol
• Collecting, recording, and reporting clinical data and findings appropriately in CRFs and collaborating with the investigator on study-related adverse events and serious adverse events according to the study protocol
• Coordinating with the study monitor on study issues and effectively responding to questions posed by the monitor.

We are looking for candidates with the following skills and experience:

• At least two years of relevant experience; or an equivalent combination of medical education, training, and experience 
• Knowledge of clinical studies combined with solid knowledge of department-, protocol-, and study-specific workflows, consent forms, and study plans
• Strong IT skills, experienced in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills with the ability to build and maintain effective working relationships
• Very good German language skills, both spoken and written

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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