Clinical Research Nurse Coordinator

hace 3 semanas


Madrid, Madrid, España Course A tiempo completo

Company Overview

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IQVIA is a leading industry company with opportunities in clinical research. We are looking for a Clinical Research Nurse and Study Coordinator to join our team in Madrid.

Job Description

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We are seeking a highly skilled Clinical Research Nurse and Study Coordinator to support two projects in Madrid, working 20 hours per project. The projects are planned for 12 months and will involve supporting two sites in conducting a clinical trial. As a pivotal member of the site team, you will be involved with various administrative tasks to ensure the smooth running of clinical trials and assist with collecting patient data.

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Your day-to-day responsibilities will include:

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  • Supporting clinical research studies and maintaining a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.">
  • Performing patient vital signs, ECGs, and blood withdrawals.">
  • Safeguarding the well-being of subjects, acting as a volunteer advocate, and addressing subjects' concerns.">
  • Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.">
  • Planning and coordinating logistical activity for study procedures according to the study protocol.">
  • Performing clinical set-up and preparation for the study, including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues.">
  • Assisting with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.">
  • Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.">
  • Correct custody of study drug according to site standard operating procedures.">
  • Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions.">
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Required Skills and Qualifications

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

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  • Bachelor's or Master's degree in life sciences or an educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g., clinical research coordinator, nurse, medical assistant, or other medical profession.">
  • Experience performing patient vital signs, ECGs, and blood withdrawals.">
  • Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.">
  • Basic knowledge of medical terminology.">
  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.">
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.">
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Salary and Benefits

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We offer a competitive salary range of €45,000 - €60,000 per year, depending on experience. Our benefits package includes access to training and development opportunities, comprehensive health insurance, and a generous paid time off policy.

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About IQVIA

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IQVIA is a leading provider of advanced analytics, technology solutions, and contract sales and marketing services to the healthcare and life science industries. We have a strong presence in Madrid and are committed to delivering high-quality services to our clients.

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How to Apply

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Please submit your application, including your resume and cover letter, through our website. We look forward to reviewing your application.


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