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Clinical Research Assistant

Minnesota Jobs - St Paul, MN

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Job Description

Clinical Trial Coordinator This position is responsible for the timely completion of case report forms, completion or facilitation of all sponsor produced queries, performance of quality control checks of case report forms prior to sponsor review, screening patient medical charts for study recruitment, acting as primary liaison for the coordinators during monitoring visits, and providing overall support for the clinical trials department. Location: Midway Corporate Campus 1700 University Ave W 55104 Schedule: 1.0FTE This is a mobile position (onsite at Cancer Care Clinic locations with the ability to work remote) Monday - Friday, 8:00AM - 4:30PM. Flexibility to schedule if needed. Represents data management at all internal and external meetings and provides data management updates as required Performs additional quality control checks prior to case report form completion Utilizes the electronic health records system to screen patient charts for study eligibility Schedules and oversees Clinical Research Associate's monitoring visits Completes closure forms and packaging of source documents and case report forms at conclusion of assigned study Reviews subjects' research charts for completion of case report forms Completes or facilitates the completion of sponsor initiated data queries Participates in the review of source documents Participates in internal and external audits as required Provides support to and takes work direction from the Study Coordinators, Principal Investigators and Business Coordinator, and performs other duties as assigned Recognizes, exemplifies and adheres to Fairview's values, which center on our commitment to Dignity, Integrity, Service and Compassion Required Qualifications 1 year experience in a healthcare setting or 1 year experience in clinical research Excellent customer service skills, proficient in the English language, good attention to detail, ability to problem solve effectively, ability to follow policies and procedures and excellent communication skills Experience using Microsoft Office tools Preferred Qualifications Experience in an oncology healthcare setting or 1 experience with oncology clinical trials Experience working with electronic medical records

Created: 2026-03-13

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