Clinical Site Monitor I/ II

vor 4 Wochen

REMOTE, Deutschland Parexel Vollzeit

Parexel FSP is currently hiring for a homebased Clinical Site Monitor I or II.

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

Experience required:

A minimum of 1 year experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite). Site activation experience Feasibility and site management experience. CRO oversight experience Submissions experience (will not be submitting as part of this role). 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. Apply today #LI-TA1
#LI-REMOTE

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