Clinical Trials Coordinator

hace 9 horas


Alcobendas, Madrid, España Parexel A tiempo completo
Overview

Parexel FSP is a leading clinical research organization dedicated to helping clients accelerate the discovery and development of new treatments.

Estimated Salary

$55,000 - $75,000 per annum (based on location and experience)

Job Description

We are seeking an experienced Site Monitor in Spain to join our clinical operations team. As a Site Monitor, you will be responsible for ensuring the successful conduct of clinical trials at assigned sites. Your duties will include:

  • Monitoring study progress and identifying any issues or concerns
  • Conducting site visits to ensure compliance with Good Clinical Practice (GCP) guidelines
  • Collecting and managing site data and documentation

You will work independently, utilizing your excellent time management and social skills to manage multiple projects simultaneously. A highly motivated individual with a keen eye for detail is required.

Required Skills and Qualifications

To be successful in this role, you will need:

  • Bachelor's degree in a life science or related discipline
  • Minimum 1.5 years' experience in independent site monitoring - all types of visits
  • Oncology experience
  • Understanding of ICH GCP Compliance
  • Excellent time management and social skills
  • Highly motivated with a phenomenal eye for detail
Benefits

We offer a competitive salary, long-term projects, world-class technology, and training tailored to your individual experience. As a Site Monitor, you will have the opportunity to work on oncology studies that deliver real impact.



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