Research Study Assistant II Sleep Medicine

Henry Ford Health; Novi (MI); On-site; USD 52,000 - 76,000; Full time

Job summary

Henry Ford Health in Novi, MI, is seeking a detail-oriented Research Study Assistant II to support our Sleep Medicine research team. You will manage data collection, documentation, and preliminary analyses while ensuring compliance with study protocols and regulatory requirements.

You will assist with PSG data collection, literature reviews, and coordination with clinical staff and participants to meet study milestones. Strong analytical skills and teamwork are essential.

Qualifications

• Experience in research support or clinical data collection.
• Strong data management and documentation practices.
• Ability to analyze and interpret research data.
• Familiarity with sleep medicine terminology and PSG data collection.
• Excellent attention to detail and time management.
• Strong written and verbal communication skills.

Responsibilities

• Assist in designing and implementing sleep medicine research methodologies, including PSG data collection and study protocols.

Skills

Data collection

Data management

Statistical analysis

Research support

Attention to detail

Regulatory compliance

Communication skills

Team collaboration

Sleep medicine knowledge

Documentation practices

Education

Bachelor's degree in life sciences or related field

Tools

SPSS

R

Python

Sleep study software

Databases

Job description

Job Description

We're looking for a detail-oriented and compassionate Research Study Assistant II to join our Sleep Medicine research team in Novi, Michigan. In this role, you will provide essential support to our sleep medicine research initiatives by managing data collection, maintaining accurate documentation, and assisting with the analysis and interpretation of research findings. The successful candidate will demonstrate strong analytical skills, attention to detail, and the ability to work efficiently within a collaborative research environment while adhering to established protocols and regulatory requirements specific to sleep medicine research.

• Assist in designing and implementing sleep medicine research methodologies, including polysomnography (PSG) data collection procedures and clinical study protocols
• Collect, organize, and maintain research data using appropriate documentation systems, databases, and sleep-specific data management tools
• Perform data entry, verification, and quality assurance to ensure accuracy and completeness of sleep study records and participant information
• Support data analysis activities by preparing datasets, running statistical analyses, and generating preliminary reports related to sleep medicine findings
• Maintain detailed and accurate records of all research activities, including participant consent forms, sleep assessments, study progress, and regulatory documentation
• Assist in literature reviews and compile relevant sleep medicine research materials to support ongoing studies
• Coordinate with research team members, clinical staff, and study participants to ensure timely completion of study milestones and deliverables
• Monitor compliance with institutional policies, ethical guidelines, and regulatory requirements specific to sleep medicine research throughout the study process
• Prepare research summaries, presentations, and documentation for team meetings and stakeholder communications
• Troubleshoot data-related issues and implement corrective actions as needed to maintain data integrity
• Support the preparation of grant proposals, progress reports, and other research documentation related to sleep medicine studies
• Demonstrate empathy and professionalism when interacting with study participants, ensuring their comfort and understanding throughout the research process

Qualifications

• Proven experience in research support, data collection, or laboratory/clinical research environments, preferably in sleep medicine or related fields
• Strong proficiency in data management, organization, and documentation practices
• Demonstrated ability to analyze and interpret research data accurately
• Solid understanding of research methodologies and study design principles
• Excellent attention to detail with strong organizational and time management skills
• Proficiency with computer systems and data management software
• Strong written and verbal communication skills
• Ability to work independently and collaboratively within a research team
• Knowledge of compliance, regulatory requirements, and ethical standards in research
• Familiarity with sleep medicine terminology, concepts, and sleep disorder assessment tools
• Experience with sleep study protocols or polysomnography (PSG) data collection and analysis
• Experience working with patient populations in clinical or research settings
• Understanding of sleep-related regulatory requirements and ethical considerations in human subjects research
• Familiarity with statistical analysis software (such as SPSS, R, or Python) – preferred
• Experience with research databases and literature management tools – preferred
• Project management experience or demonstrated ability to manage multiple tasks simultaneously – preferred
• Background in grant writing or proposal development – preferred