Oncology Clinical Research Coordinator — Madrid (Part-Time)

IQVIA

Madrid

Presencial

EUR 25.000 - 39.000

A tiempo parcial

Hace 12 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

IQVIA in Madrid is seeking a part-time Clinical Research Coordinator to support an oncology trial on site, up to 18 hours per week for six months. This pivotal role involves assisting investigators, safeguarding subject safety, and ensuring smooth trial operations in a busy site environment.

You will handle study documentation, enrollment activities, data entry, and coordination with monitors and stakeholders, contributing to data quality and patient safety while adhering to study protocols and

Formación

  • BS/BA in life sciences or equivalent and relevant experience.
  • At least three years in oncology clinical trials.
  • Strong knowledge of trial processes, CRFs, and study protocols.

Responsabilidades

  • Support clinical studies and maintain a safe study environment.
  • Safeguard subjects' wellbeing and address concerns.
  • Maintain study documents, CRFs, and EDC systems.
  • Plan and coordinate procedures according to protocol.
  • Assist with data entry, quality checks, and queries.
  • Assist in enrollment by screening volunteers.
  • Ensure correct custody of study drug per SOPs.
  • Coordinate with study monitor on issues.

Conocimientos

Clinical coordination
Oncology trials
Data entry
CRF management
MS Office

Educación

BS/BA in life sciences

Herramientas

EDC systems
MS Excel
MS Word

Descripción del empleo

IQVIA in Madrid is seeking a part-time Clinical Research Coordinator to support an oncology trial on site, up to 18 hours per week for six months. This pivotal role involves assisting investigators, safeguarding subject safety, and ensuring smooth trial operations in a busy site environment.

You will handle study documentation, enrollment activities, data entry, and coordination with monitors and stakeholders, contributing to data quality and patient safety while adhering to study protocols and

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