Clinical Trials Coordinator
hace 9 horas
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 DescriptionWe 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 QualificationsTo 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
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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