Clinical Research Nurse and Study Coordinator

hace 10 horas

Madrid, Madrid, España Iqvia Argentina A tiempo completo
Job Title: Clinical Research Nurse and Study Coordinator

We are seeking a highly skilled Clinical Research Nurse and Study Coordinator to join our team at IQVIA Argentina. As a pivotal member of our site team, you will be involved in a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials.

Key Responsibilities:
  • Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.
  • Perform patient vital signs, ECGs, and blood withdrawals.
  • Safeguard the well-being of subjects, act as a volunteer advocate, and address subjects' concerns.
  • Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
  • Plan and coordinate logistical activity for study procedures according to the study protocol.
  • Perform 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.
  • Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
  • Assist 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.
  • Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
Requirements:
  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession.
  • 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.
  • Good organizational skills with the ability to pay close attention to detail.

Why work with us?

We offer a dynamic and challenging work environment that allows you to grow and develop your skills. If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply for this exciting opportunity.

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