Part-Time Clinical Research Coordinator - Data & Trials

IQVIA

Málaga

Presencial

EUR 21.000 - 34.000

A tiempo parcial

14 días+
Generador de candidaturas

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Descripción de la vacante

IQVIA is seeking a part-time Clinical Research Coordinator in Málaga to support a single site with 10 hours per week. You will assist investigators, manage study documents, and help ensure protocol adherence and data quality.

The role requires a life sciences background, familiarity with clinical trials, and strong IT and interpersonal skills to coordinate with the study team and volunteers.

Formación

  • BS/BA in life sciences or equivalent and/or relevant clinical experience.
  • Basic knowledge of clinical trials and study procedures.
  • Strong IT skills with MS Office.
  • Excellent interpersonal and organizational skills.
  • Ability to recruit, screen and orient volunteers per protocol.

Responsabilidades

  • Support clinical research studies and maintain a safe study environment.
  • Safeguard the well-being of subjects and address concerns.
  • Maintain study protocols, CRFs, EDC systems and related documents.
  • Plan and coordinate logistical activity for study procedures.
  • Prepare for study procedures including labeling tubes and inventory.
  • Assist with data entry, quality checks and query resolution.
  • Assist in study enrollment by recruiting and screening volunteers.
  • Ensure correct custody of study drug per SOPs.
  • Coordinate with study monitor and respond to questions.

Conocimientos

IT proficiency
Interpersonal skills
Organizational skills
Attention to detail

Educación

BS/BA in life sciences or equivalent

Herramientas

MS Windows
MS Excel
MS Word
Access

Descripción del empleo

IQVIA is seeking a part-time Clinical Research Coordinator in Málaga to support a single site with 10 hours per week. You will assist investigators, manage study documents, and help ensure protocol adherence and data quality.

The role requires a life sciences background, familiarity with clinical trials, and strong IT and interpersonal skills to coordinate with the study team and volunteers.

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