Clinical Research Associate I/II

Vor 3 Tagen

Berlin, Berlin, Deutschland Parexel Vollzeit

Transforming Patients' Lives through Innovative Clinical Research

Parexel FSP is seeking a highly skilled Clinical Site Monitor I or II to join our team. As a single sponsor dedicated to a worldwide biopharmaceutical company, we relentlessly seek breakthroughs to improve patients' lives.

The ideal candidate will be responsible for ensuring data integrity and quality, as well as compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line with the Study Monitoring Plan (SMP) and will be performed virtually for most activities to supplement on-site visit requirements.

Key Responsibilities:

  • Collaborate with the Site Manager to ensure the site follows the protocol and is inspection-ready.
  • Coordinate with institutions and investigators at the local level.
  • Utilize systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), and electronic Investigator Site File (eISF).
  • Ensure a minimum of 1 year experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite).
  • Oncology trials experience is required.
  • Bachelor's degree or Registered Nurse (RN) in a related field or equivalent combination of education, training, and experience.

We Offer:

Exceptional financial rewards, training, and development opportunities. A healthy work-life balance and a commitment to your welfare, just as highly as that of our patients.

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