Clinical Research Nurse

hace 4 días

Valladolid, Valladolid, España Iqvia A tiempo completo

We are seeking a skilled Clinical Research Nurse to join our team in Segovia. This part-time (24 hours) role is an excellent opportunity for individuals who want to work in clinical research and contribute to the success of IQVIA.

About the Role

This 12-month contract will involve supporting our site team in conducting a clinical trial. As a pivotal member of the team, you will be responsible for various administrative tasks, including:

  • Supporting clinical research studies and maintaining a safe study environment according to health and safety policies under the direction 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.

Your day-to-day responsibilities will also include maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents. You will plan and coordinate logistical activity for study procedures according to the study protocol and perform clinical set-up and preparation for the study.

Key Responsibilities
  • 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.
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.

Requirements

To be successful in this role, you will need:

  • A BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
  • 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.
What We Offer

We offer a competitive salary of €40,000 per annum, which reflects the specific requirements and qualifications for this role. Additionally, we provide a range of benefits, including opportunities for professional development and growth within the company.

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