Clinical Research Associate II, Phase I

Fortrea • Durham, NC, US • published 2026-09-23 11:43:00.910849

Description

**Our Phase I team is currently seeking a** **Clinical Research Associate II with 1\+ years of on\-site monitoring experience.** **Ideal candidates would have phase I experience and reside within the U.S.** **WHAT YOU WILL DO** You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards. **Responsibilities** : * Responsible for all aspects of study site monitoring including routine monitoring and close\-out of clinical sites, maintenance of study files, conduct of pre\-study and initiation visits; liaise with vendors; and other duties, as assigned \- * Responsible for all aspects of site management as prescribed in the project plans * General On\-Site Monitoring * Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study * Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements * Ensure the integrity of the data submitted on Cas...

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