CRA Level I
Employer · ThermoFisher Scientific
Remote
Join Us as a Clinical Research Associate I -- Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process.
Tasks
- Perform and coordinates different aspects of the clinical monitoring and site management process.
- Conduct remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.
- Manage procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.).
- Act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
- Ensure audit readiness. Develops collaborative relationships with investigational sites.