GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Cancer Center Protocol Office is seeking motivated, detail-oriented individuals to join our team as a Clinical Research Associate. The Cancer Center Protocol Office is a centralized research office that supports clinical researchers in all disciplines within the Cancer Center. Our office promotes and facilitates clinical research by providing comprehensive services to physicians conducting clinical trials while ensuring compliance with all regulatory requirements.

The Clinical Research Associate I (CRA I) works under general supervision to enroll eligible patients to clinical research protocols and manage data collection and regulatory submissions for multiple cancer studies. The CRA I will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. The CRA I will be trained on the institutional and federal regulations governing clinical research. The position involves a high volume of data abstraction and data entry. This position does not include any direct patient contact.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

The CRA I will perform the following data management duties under general supervision by the Clinical Research Manager:

• Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all inclusion/exclusion criteria

• Enroll patients as required by the study sponsor and internal enrollment monitor team

• Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance

• Complete data entry as required for individual study protocols ensuring compliance with institutional and regulatory requirements.

• Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulation

• Maintain research charts and/or electronic files for all enrolled patient

• Ensure adequate source documentation is in place for all data reported

• Resolve data queries issued by the sponsor

• Obtain protocol clarifications from the study sponsor and communicate information to the research team

• Schedule and prepare for monitoring visits with sponsor

• Facilitate the request and shipment of archival pathology sample

• Organize and prepare for internal and external audit

• Maintain ongoing communication with clinical team regarding study patients and progress for multiple studie

The following regulatory duties may be performed under general supervision by the Clinical Research Manager:

• Maintain and organize study specific regulatory binder

• Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB

• Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study

• Manage adverse event and deviation/violation/exception documentation for all enrolled patients and report to the sponsor and IRB as required

• Submit Data and Safety Monitoring Report

• Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial proce

• Collect, complete, and submit essential regulatory documents to various regulatory entitie

• Participate in monitoring visits and file all monitoring visit correspondence

• Ensure appropriate documentation of delegation and training for all study staff member

• Maintain screening and enrollment log

SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:

• Careful attention to detail

• Good organizational skill

• Ability to follow direction

• Good communication skill

• Computer literacy

• Working knowledge of clinical research protocol

• Ability to demonstrate respect and professionalism for subjects rights and individual need

Qualifications

EDUCATION:

• BA/BS degree required

EXPERIENCE:

• None

SUPERVISORY RESPONSIBILITY:

• None

WORKING CONDITIONS:

• Duties may be performed in a combination of on-site and remote work setting