Apply on Employer Site

Cairns Health · 21 hours ago

Part-Time Research Coordinator - Health Technology

Sunnyvale, CA

Full-time, Part-time

Onsite

Entry Level

1+ years exp

Cairns Health is a cutting-edge health technology company developing Luna, a device designed to improve healthcare outcomes for seniors. They are seeking a Part-Time Research Coordinator to support a large-scale data collection study by coordinating test subject acquisition, overseeing study execution, and ensuring data integrity.

Consumer ElectronicsElder CareHealth CareHome Health Care

Responsibilities

Participant recruitment & coordination

Identify and recruit 200 study participants from diverse demographic groups, including seniors in independent living and assisted living facilities

Screen potential participants to ensure eligibility based on study criteria

Coordinate participant schedules for study sessions and manage consent forms

Serve as the primary point of contact for participants, addressing any concerns and ensuring compliance with study protocols

Study Execution & Data Collection

Setup and calibrate Luna devices, infrared cameras, 3D tracking systems, and wearables in test environments

Guide participants through the study protocol, including movement tasks, sleep tracking, and real-world interaction with the device

Monitor participants during daytime movement assessments and overnight data collection

Ensure protocol adherence by verifying that participants follow scheduled activities

Maintain detailed logs of participant activities, device placements, and any deviations from protocol

Data Management & Quality Control

Oversee the collection, labeling, and storage of sensor data from multiple devices

Work with the research team to ensure proper syncing of wearable data with radar-based monitoring

Conduct initial data reviews to detect anomalies and coordinate with engineers for troubleshooting

Maintain strict confidentiality and ethical standards in handling participant information

Equipment Management & Setup

Set up and test all study equipment, including radar-based sensors, infrared cameras, and auto-labeling tools

Perform routine device maintenance, troubleshooting, and firmware updates

Ensure proper power supply, camera positioning, and data recording integrity for each study session

Compliance & Ethical Oversight

Ensure all study activities adhere to Institutional Review Board (IRB) guidelines, HIPAA regulations, and participant privacy requirements

Provide participants with study debriefs and ensure proper informed consent documentation

Qualification

Clinical research experienceBiomedical equipment setupData management skillsParticipant recruitmentHuman subject research regulationsCommunication skillsOrganizational skillsProblem-solving ability

Required

Bachelor's degree in a relevant field (e.g., Biomedical Engineering, Psychology, Neuroscience, Public Health, Clinical Research, or a related discipline)

1-3 years of experience in human subject research, clinical trials, or healthcare studies

Experience with participant recruitment and protocol execution

Strong technical aptitude with experience in setting up and operating biomedical or sensor-based research equipment

Excellent organizational and data management skills

Ability to work independently and problem-solve in a research setting

Strong communication and interpersonal skills, especially when working with elderly participants