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FSP Experienced Clinical Research Associate (CRA II/Sr. CRA I) - Oncology - Respiratory - Cardiovascular - US West

Thermo Fisher Scientific • OR, US • published 2026-11-06 00:59:38.725242

Description

**Work Schedule** Standard (Mon\-Fri)**Environmental Conditions** Office**Job Description** **Purpose:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on\-site visits to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts 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. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task matrix. **Essential Functions and Other Job Information:** **Major Job** **Responsibilities** * Monitors investigator sites with a risk\-based monitoring approach. * Applies root cause analysis (RCA), critical thinking and problem\-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decreas...

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