Clinical Research Coordinator

Vor 5 Tagen

Frankfurt am Main, Hessen, Deutschland IQVIA Vollzeit
About the Role

We are seeking a highly skilled and experienced Clinical Research Coordinator to join our team at IQVIA. As a Clinical Research Coordinator, you will play a critical role in the success of our clinical studies, ensuring that all aspects of the study are conducted in accordance with the protocol and regulatory requirements.

Key Responsibilities
  • Coordinate clinical research studies and maintain a safe study environment in accordance with health and safety guidelines under the supervision and delegation of the Principal Investigator.
  • Ensure the well-being of participants, represent the interests of volunteers, and ensure the highest quality of care while maintaining the confidentiality of participant information.
  • Better manage participant relationships and support staff with administrative tasks.
  • Maintain study protocols, case report forms (CRFs), electronic data capture systems (EDC), and other study documents up-to-date.
  • Plan and coordinate logistical activities for study procedures in accordance with the study protocol.
  • Conduct clinical preparations for the study, including labeling of sample tubes and containers, inventory of required materials, and setting up or resolving issues with equipment and/or the study.
  • Assist with data entry, data quality checks, and answering questions to ensure the study protocol is followed and quality control is maintained.
  • Support participant recruitment, screening, and enrollment in the study in accordance with the study protocol.
  • Collect, record, and report clinical data and findings in a suitable manner and collaborate with the Principal Investigator to report study-related adverse events and serious adverse events in accordance with the study protocol.
  • Coordinate with the study monitor to address study issues and effectively respond to questions from the monitor.
  • Perform a variety of complex clinical procedures on participants, including but not limited to vital signs, blood draws, administration of IP, ECG, etc.
Requirements
  • At least one year of relevant experience; or an equivalent combination of medical education, training, and experience.
  • Knowledge of clinical studies combined with a solid understanding of departmental, protocol, and study-specific workflows, informed consent, and study plans.
  • Experience in blood draws and ECG is required.
  • Proficient in IT skills, experienced in working with 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.
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://www.iqvia.com/

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