Clinical Research Coordinator I

JOB REQUIREMENTS: Position Description: Purpose Perform the day-to-day

administrative activities of the clinical research trials program.

Provide support to the team to facilitate the achievement of the

program's goals. Primary Functions Recruit, screen, enroll and obtain

consent from program participants. Conduct or coordinate training for

program participants. Coordinate research protocols including arranging

necessary appointments and procedures, working collaboratively with

other departments and institutions, and maintaining contact with study

participants. Maintain patient calendars, screening and enrollment

information utilizing the OnCore software tool to assist in patient

specific protocol required timelines to ensure compliance with protocol

requirements. Monitor the study related activities on a patient and

protocol level. Collect, analyze, and disseminate program data. Report

program data and progress to program stakeholders. Identify problems or

obstacles in the system/procedures related to implementation of the

research protocols and communicate to the study investigators. Assure

compliance with all relevant IRB and other regulatory agency

requirements. Assist in the preparation of IRB documents and reports.

Assist in the evaluation and writing of research protocols. Collaborate

on the development of program materials including educational materials,

marketing materials, websites, forms, and reports. Work with Principal

Investigator to develop, implement, and maintain comprehensive databases

and files related to the program. Maintain program timeline including

tracking deadlines for program components. Coordinate program outreach

activities including acting as a liaison with community organizations.

Work with CTO Beacon Coordinator, and entire Beacon review team, to

assist with protocol specific ordering system requirements to assure

protocol compliance. Assist in the preparation of IRB documents and

reports. Facilitate monitoring and audit related activities. Process and

ship lab specimens as necessary. Knowledge - Skills - Abilities

Knowledge of biology, chemistry, mathematics, documentation, and records

management. Data utilization, complex problem solving, critical

thinking, resource management, and writing skills. Preferred Schedule:

M-F 8-4:30 Position Requirements: Specifications Appropriate experience

may be substituted on equivalent basis Minimum Required Education:

Associate's Degree Minimum Required Experience: 1 year of experience in

research Preferred Education: Bachelors degree Preferred Experience:

Experience with clinical research in a medical research or For full

info follow application link. EEO/AA Minorities/Females/Vets/Disability

The Medical College of Wisconsin is an affirmative action/equal

opportunity employer and does not discriminate in hiring or employment

on the basis of age, sex, race, color, religion, national origin,

veteran status, disability or sexual orientation. APPLICATION

INSTRUCTIONS: Apply Online: ipc.us/t/948B25EE03554490 Qualified females,

minorities, and special disabled veterans and other veterans are

encouraged to apply.