Clinical Research Assistant will perform recruitment activities to identify potential research participants who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients. Escorts participants from one study activity to another; cleans research equipment; assists with collecting, extracting, coding and analyzing clinical research data; completes data entry, scans research records; generates reports and reviews to ensure validity of data supports activities to ensure compliance with all Institutional Review Boards (IRB).

If you are passionate about healthcare and supporting patients, this remote position may be for you. You will respond to prescription refill requests, verify accuracy, prepare refills, provide customer service, analyze data, adhere to schedules and provide administrative support.

The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Frontline liaison between the sponsor and sites to ensure successful collaboration.