Clinical Operations Specialist

hace 4 semanas


Alcobendas, Madrid, España Parexel A tiempo completo

About the Role

Parexel FSP is seeking a skilled Site Monitor to join our clinical operations team in Spain (Madrid or Barcelona). As a Site Monitor, you will work independently to set up and oversee studies, complete study status reports, and maintain study documentation.

Key Responsibilities

  • Participate in the submission of protocols, consent documents for ethics/IRB approval, and assist in the preparation of regulatory submissions as requested.
  • Work with world-class technology and training tailored to your individual experience.
  • Collaborate with a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact.

Requirements

  • Bachelor's degree in a life science or related discipline.
  • Minimum of 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.
  • Ability to travel domestically and internationally approximately 65%-75% of working time.
  • Current driver's license required.


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