US National Labor Exchange Home
Clinical Research Coordinator I - MILWAUKEE, WI,

Job Information

Job Order ID :
WI3655282
# of Positions :
1
Minimum Education Level :
Vocational Degree
Experience Required :
Training :
Associate Degree
Duration :
Shift :
Unspecified
Hours per week:
40

Job Description

 
JOB REQUIREMENTS: Position Description: Clinical Research Coordinator I
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: Fulltime 8-4:30 Position
Requirements: Specifications Appropriate experience may be substituted
for education on an equivalent basis Minimum Required Education:
Associate\'s Degree Minimum Required Experience: 1 year of experience in
research. Preferred Education: Bachelors degree Preferred
Experience:\... 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/E74DB39838CE426E Qualified females, minorities, and special
disabled veterans and other veterans are encouraged to apply.

Company Information

Name :
MCW: SARGEANT HEALTH CENTER

Application Information

© 2024 Copyright DirectEmployers Association, Inc., a non-profit consortium of leading global employers