Clinical Research Coordinator

hace 2 semanas


Valencia, Valencia, España IQVIA A tiempo completo
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.


This part-time (20 hours) role, is planned for 3 months and is to support the site in
Alzira, Valencia in conducting a clinical trial in the field of
Endocrinology.


As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.


Day to day responsibilities will include:

  • 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
  • Maintain uptodate study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Plan and coordinate logístical activity for study procedures according to the study protocol
  • Perform clinical setup 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 monitorinitiated questions.
  • 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
  • Basic knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and client
  • Good organizational skills with the ability to pay close attention to detail.
LI-DNP

LI-CES

LI-HCPN

LI-XB1

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