Sleep Medicine Research Assistant II

Henry Ford Health

Novi (MI)

On-site

USD 42,000 - 62,000

Full time

7 days ago
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Job summary

Henry Ford Health in Novi, MI, is seeking a detail-oriented Research Study Assistant II to support sleep medicine research initiatives. You will manage data collection, documentation, and assist with analysis while ensuring adherence to study protocols and regulatory requirements.

The role involves coordinating with clinical staff and study participants, maintaining records, and contributing to literature reviews.

Qualifications

  • Proven experience in research support, data collection, or laboratory/clinical research environments.
  • Strong proficiency in data management, organization, and documentation practices.
  • Ability to analyze and interpret research data accurately.
  • Knowledge of compliance, regulatory standards, and ethical guidelines in research.
  • Experience with sleep study protocols or PSG data collection is preferred.

Responsibilities

  • Assist in designing and implementing sleep medicine research methodologies, including PSG data collection procedures.
  • Collect, organize, and maintain research data using documentation systems and databases.
  • Perform data entry, verification, and quality assurance to ensure accuracy of records.
  • Support data analysis by preparing datasets and running statistical analyses.
  • Maintain detailed records of research activities and regulatory documentation.
  • Prepare summaries, presentations, and reports for team meetings and stakeholders.

Skills

Research support
Data collection
Data management
Analytical skills
Documentation practices

Education

High School Diploma or GED
Associate degree in research or healthcare

Tools

SPSS
R
Python

Job description

Henry Ford Health in Novi, MI, is seeking a detail-oriented Research Study Assistant II to support sleep medicine research initiatives. You will manage data collection, documentation, and assist with analysis while ensuring adherence to study protocols and regulatory requirements.

The role involves coordinating with clinical staff and study participants, maintaining records, and contributing to literature reviews.

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