Clinical Research Associate I/II

vor 1 Woche

Berlin, Berlin, Deutschland Parexel Vollzeit

Transforming Patients' Lives through Innovative Research

Parexel FSP is seeking a highly skilled Clinical Site Monitor I or II to join our team.

As a dedicated single sponsor, we are committed to advancing breakthroughs in biopharmaceutical research. Our daily innovation drives us to improve patients' lives, and we are seeking like-minded individuals to join our mission.

The successful candidate will be responsible for ensuring data integrity and quality, as well as compliance with ICH GCP and local requirements at the site level. They will work closely with the Site Manager to ensure the site follows the protocol and is inspection-ready.

Key qualifications include:

  • A minimum of 1 year experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite).
  • Oncology trials experience.
  • Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF).
  • Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.

We offer competitive financial rewards, comprehensive training, and opportunities for professional growth. Our commitment to our employees' welfare is matched only by our dedication to improving patients' lives.

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