Clinical Site Monitor I/ II Position

3 settimane fa


Florence, Toscana, Italia Iiabsc A tempo pieno
Career Opportunity

We are seeking a highly skilled Clinical Site Monitor/CRA I or II to join our team at Parexel FSP. This is an exciting opportunity for a motivated individual to work in a dynamic environment, collaborating with institutions and investigators at the local level.

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 also coordinate with the Site Manager to ensure the site follows the protocol and is inspection-ready.

The ideal candidate will have a minimum of 1 year's experience as a clinical monitor, with demonstrated experience monitoring (virtual or onsite). Experience in managing complex protocols in Oncology or other therapeutic areas where protocols are determined to be high risk is also required.

Key Responsibilities:

  • Ensure data integrity and quality
  • Compliance with ICH GCP and local requirements
  • Coordinate with Site Manager to ensure site protocol adherence
  • Manage complex protocols in Oncology or other therapeutic areas

Requirements:

  • Bachelor's degree or Registered Nurse (RN) in a related field
  • Minimum 1 year's experience as a clinical monitor
  • Experience in utilizing systems like Siebel Clinical Trial Management System (CTMS), electronic Trial Master File (eTMF), electronic Investigator Site File (eISF) (Florence)

Compensation and Benefits:

We offer competitive financial rewards, including an estimated annual salary of $60,000 - $80,000, depending on experience. We also provide opportunities for training and development, as well as a healthy work-life balance.

About Us:

Parexel FSP is a leading provider of clinical trial management services. We are committed to improving patients' lives through groundbreaking solutions and innovative approaches.



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