Clinical Operations Specialist

hace 3 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.
  • Develop your career with us by contributing your personal and professional talents and skills.

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.

About Us

Parexel FSP is a leading clinical research organization dedicated to delivering innovative solutions for the pharmaceutical and biotechnology industries. We appreciate our team's dedication and commitment to excellence, and we work with heart, keeping the patient at the center of everything we do.



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