Clinical Research Coordinator- Barcelona Part Time - IQVIA

IQVIA
IQVIA
Empresa verificada
Barcelona, España

hace 2 días

Isabel García

Publicado por:

Isabel García

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Descripción

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Assistant.


This role,
planned
for one year part-time (25h per week), is to support the site in
Barcelona in conducting a clinical trial.


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:

  • Coordinate 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
  • Collect, record, and report clinical data and findings appropriately in CRFs while collaborating with study investigator about studyrelated adverse events and serious adverse events according to the study protocol
  • Coordinate with study monitor on study issues and effectively respond to monitorinitiated questions.
  • BS/BA in life sciences or educational equivalent and relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
  • Knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
  • 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.
  • Spanish speaker with good English skills
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