Clinical Research Associate I/II

Vor 6 Tagen

Berlin, Berlin, Deutschland Parexel Vollzeit

Transforming Patients' Lives through Groundbreaking Solutions

Parexel FSP is seeking a dedicated 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.

Our daily innovation contributes to a healthier global community. This is where today's visionaries, solution-seekers, and trailblazers converge to shape tomorrow's groundbreaking solutions. Together, we have the power to revolutionize patients' well-being.

The Site Monitor will be responsible for data integrity and data quality, ensuring 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.

The Site Monitor will collaborate with the Site Manager to ensure that the site follows the protocol, and is inspection-ready, and will coordinate with institutions and investigators at the local level.

Key Responsibilities:

  • 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), electronic Investigator Site File (eISF) (Florence).
  • 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. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

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