Job Description
Parexel are currently recruiting for a sponsor dedicated Site Monitor in Norway.
Previous oncology trials experience is essential.
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 the majority of activities to supplement on site visit requirements. The Site Monitor will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready and will coordinate with institutions and investigators at the local level.
**Some specifics about this advertised role**
**_ Oversight of Monitoring Responsibilities and Study Conduct_**
- Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific acti...
Previous oncology trials experience is essential.
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 the majority of activities to supplement on site visit requirements. The Site Monitor will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready and will coordinate with institutions and investigators at the local level.
**Some specifics about this advertised role**
**_ Oversight of Monitoring Responsibilities and Study Conduct_**
- Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific acti...