Clinical Research Coordinator Assistant

at  University of Michigan

HOW TO APPLY

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

JOB SUMMARY

The Department of Psychiatry seeks a dedicated and detail-oriented individual to join our growing research team. The Clinical Research Assistant will play a pivotal role in recruiting participants and conducting on-site sleep study operations. This position offers invaluable experience in research areas such as substance use and sleeping disorders. Additionally, the position provides excellent opportunities for career development, learning, and competitive benefits.

REQUIRED QUALIFICATIONS*

• High school diploma or GED.
• The ability to prioritize multiple tasks and meet deadlines are critical.
• The ability to adhere to strict confidentiality guidelines is a necessity.
• Must be able to work nights and weekends on a regular, weekly-basis.
• Must be able to work independently for extended periods of time while receiving feedback and guidance from project leadership.

DESIRED QUALIFICATIONS*

• This project will serve a widespread and complex population. Ability to work with a diverse range of participants.
• The job will require flexibility to meet project deadlines and goals; therefore, the ability to problem solve and openness to change is highly desired.
• Previous experience with clinical research or substance use/alcohol use populations.
• Experience with data platforms (e.g., RedCap).

Knowledge of all 8 competency domains is expected:

• Scientific Concepts and Research Design
• Ethical Participant Safety Considerations
• Investigational Products Development and Regulation
• Clinical Study Operations (GCP’s)
• Study and Site Management
• Data Management and Informatics
• Leadership and Professionalism
• Communication and Teamwor

Knowledge of all 8 competency domains is expected:

• Scientific Concepts and Research Design
• Ethical Participant Safety Considerations
• Investigational Products Development and Regulation
• Clinical Study Operations (GCP’s)
• Study and Site Management
• Data Management and Informatics
• Leadership and Professionalism
• Communication and Teamwork

Position Specific Responsibilities will Include :

• Conduct participant recruitment, screening, and obtain informed consent. Track recruitment efforts in the study database.
• Coordinate and conduct baseline and follow-up assessments, including material preparation, participant scheduling, assessment administration, and coordination with study therapists.
• Assist with on-site sleep study operations, including participant scheduling, check-in, and equipment setup, with a requirement for regular night and weekend shifts.
• Provide support to the project by handling administrative tasks including data entry, documenting participant activities, preparing study materials, communicating with participants, and accurately following research protocols.
• Attend and prepare for study team meetings.