Clinical Study Coordinator

hace 1 mes


Madrid, Madrid, España Icon Plc A tiempo completo
Company Overview

ICON plc is a leading healthcare intelligence and clinical research organization, driving innovation and excellence in the industry.

Job Summary

We are seeking an experienced Clinical Study Coordinator to join our team. As a Clinical Study Coordinator, you will be responsible for managing and implementing clinical studies, working closely with a global team to achieve project goals.

Responsibilities:
  • Identify, train, and initiate study sites
  • Conduct remote site monitoring visits and/or targeted on-site visits as needed
  • Train site staff on essential processes and systems
  • Collect and manage essential documents
  • Manage study sites and required protocols, amendments, and deviations, ensuring accurate data reporting and timely completion
Requirements:
  • Clinical or life science degree (e.g., Bachelor or Master of Biology, Chemistry, Biochemistry, Biomedicine, Pharmacy, Pharmacology)
  • At least 2 years of previous site management and/or monitoring experience, ideally as a CRA or In-house CRA
  • Great command of French and English; any additional language is a plus
  • Experience working within a CRO, Pharmaceutical, or hospital/healthcare environment
Benefits

We offer a competitive salary: £45,000 per annum. Our benefits package includes:

  • Variety of annual leave entitlements
  • A range of health insurance options
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme
  • Flexible country-specific optional benefits

We are committed to fostering an inclusive environment that values diversity and promotes equal opportunities for all employees. We welcome applications from individuals who share our vision and values.


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