Clinical Research Coordinator

hace 3 semanas

Madrid, España IQVIA A tiempo completo

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator / Study Nurse to support a site in Villamartin.

This part-time role is for 24 hours per week and is expected to last approximately 1 year. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

  • Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Performing ECG and vital signs
  • Planning and coordinating logistical activity for study procedures according to the study protocol
  • 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
  • Ordering and maintaining study supplies

We are looking for candidates with:

  • 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, Research Assistant, nurse, medical assistant, other medical profession
  • Experience conducting ECG and taking vital signs
  • Good 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
  • Fluent Spanish and English language skills

If this sounds like the perfect opportunity for you, please apply now

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