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Temporary Sleep Study Participant Jobs (NOW HIRING)

MedBridge Healthcare LLC

Sleep Technologist

Northfield, MN · On-site

$26.75 - $36.75/hr

Pivotal Health is a leading provider of sleep laboratory management services and sleep therapy ... to study participant's procedural-related inquiries by providing appropriate information.

Holy Name

Sleep Technologist - Per Diem

Teaneck, NJ · On-site

$28 - $38.50/hr

Description Sleep Technician Holy Name is New Jersey's last remaining independent, Catholic health ... Responds to study participant's procedural-related inquiries by providing appropriate information.

Holy Name Hospital

Sleep Technologist - Per Diem

Teaneck, NJ · On-site

$28 - $38.50/hr

Description Sleep Technician Holy Name is New Jersey's last remaining independent, Catholic health ... Responds to study participant's procedural-related inquiries by providing appropriate information.

Holy Name

Sleep Technologist - Per Diem

Teaneck, NJ · On-site

$28 - $38.50/hr

Description Sleep Technician Holy Name is New Jersey's last remaining independent, Catholic health ... Responds to study participant's procedural-related inquiries by providing appropriate information.

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Temporary Sleep Study Participant information

What should I expect in terms of daily routines and interactions during a temporary sleep study participant role?

As a temporary sleep study participant, your daily routine will typically involve adhering to a set schedule that includes specific sleep and wake times, as well as following instructions regarding diet, activity, and the use of electronic devices. You may spend extended periods in a sleep clinic or research facility, where you'll be monitored by sleep technicians and researchers using various equipment. Interactions are usually structured, with staff guiding you through procedures and answering questions, but socialization with other participants may be limited to ensure study integrity. It's important to be comfortable with overnight stays and following protocols closely, as your cooperation directly impacts the quality of the research.

What is a temporary sleep study participant?

Temporary Sleep Study Participants are individuals who volunteer or are recruited to take part in scientific or medical studies that monitor sleep patterns, behaviors, and related physiological processes. These participants usually spend one or more nights in a controlled environment, such as a sleep lab, where researchers collect data using various sensors and equipment. The purpose of these studies can range from understanding sleep disorders to testing new treatments or products. Participation is typically short-term and may be compensated. No specific qualifications are usually required, though eligibility criteria may vary depending on the study.

What is the difference between Temporary Sleep Study Participant vs Sleep Technician?

AspectTemporary Sleep Study ParticipantSleep Technician
CredentialsNone required; may need basic health screeningCertification or training in sleep technology often required
Work EnvironmentResearch settings, clinics, or hospitals during sleep studiesSleep labs, hospitals, or clinics conducting sleep tests
Employer & IndustryResearch institutions, medical centersSleep centers, hospitals, healthcare providers
Search & Comparison IntentUnderstanding roles in sleep studies, participation requirementsJob duties, qualifications, and career info in sleep technology

In summary, a Temporary Sleep Study Participant is primarily involved in participating in sleep research or testing without formal credentials, while a Sleep Technician is a trained professional responsible for conducting sleep studies, often requiring certification and technical skills. Both roles are integral to sleep health but differ significantly in responsibilities and qualifications.

What are the key skills and qualifications needed to thrive as a temporary sleep study participant, and why are they important?

To thrive as a Temporary Sleep Study Participant, you need the ability to follow detailed instructions, maintain a consistent sleep schedule, and meet any specific health or demographic criteria set by the study. Understanding and complying with monitoring equipment such as polysomnography devices and wearable trackers is typically required. Reliability, patience, and clear communication with research staff are valuable soft skills for this role. These skills and qualities ensure accurate data collection and contribute to the validity and success of the research study.

What cities are hiring for Temporary Sleep Study Participant jobs?

Cities with the most Temporary Sleep Study Participant job openings:

What are the most commonly searched types of Sleep Study Participant jobs?

The most popular types of Sleep Study Participant jobs are:

What states have the most Temporary Sleep Study Participant jobs?

States with the most job openings for Temporary Sleep Study Participant jobs include:

Temporary Sleep Study Participant jobs near you
Infographic showing various Temporary Sleep Study Participant job openings in the United States as of July 2026, with employment types broken down into 2% Internship, 1% As Needed, 74% Full Time, 20% Part Time, 2% Temporary, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Study Participant Recruiter

Headlands Research

Lake Worth, FL • Remote

Full-time

Medical, Dental, Vision, Life, PTO

Re-posted 2 days ago

Job description

 Location: Remote in the United States  | Corporate  | Full-Time  | Clinical Research

We're seeking temporary full-time remote Study Participant Recruiters to help us enroll for studies over the next 90 days (approximately). There is the possibility of extending the length of time. The Patient Recruitment Specialist will work remotely and be responsible for all subject recruitment-related activities for assigned clinical trials. This includes but is not limited to mastery of protocol specific inclusion/exclusion criteria, participation in the development of recruitment strategies and plans, and the tracking of recruitment results. The Patient Recruitment Specialist will mainly be responsible for phone screening potential study participants, entering information into the clinical database, and scheduling potential participants for on-site visits.

Schedule:  Mondays through Fridays, 8:00am - 5:00pm
Location:  Remote in the United States
Reports to:  Patient Recruitment Manager
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

 Why Join Us?

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.

Responsibilities:

  • Make 60+ outbound calls a day, responding to patients that are interested in participating in a clinical trial; assess preliminary subject eligibility against protocol specific inclusion and exclusion criteria
  • Answer incoming calls from potential study patients and assess preliminary subject eligibility against protocol specific inclusion and exclusion criteria
  • Pass qualified patients onto the Sr. Patient Recruitment Specialist for more detailed medical pre-screening
  • Develop and maintain working knowledge of assigned medical indications
  • Review patient database, vendor portals and other electronic platforms as required to identify potential study patients and initiate contact
  • Ensure accurate collection and entry of patient information into the relevant databases while on the phone
  • Ensure courteous and efficient service is provided to all callers
  • Support other members of your team as well as cross-functional team members
  • Attend and contribute to department meetings
  • Performing other administrative tasks, as required.

Requirements:

  • Bilingual in English and Spanish preferred, but not required
  • Bachelor's degree, Associate's degree, or equivalent education or experience preferred
  • Prior experience delivering excellent customer service is required; call center experience a plus
  • Medical terminology knowledge a plus
  • Prior inside sales experience a plus
  • Experience with Salesforce a plus
  • Passion for communicating with people required
  • Possess exceptional organizational skills and attention to details
  • Display excellent verbal and written communication skills
  • Able to quickly adapt to changes in responsibilities, workloads and priorities
  • Be a fast learner with capacity to retain and differentiate key enrollment criteria across clinical trials
  • Demonstrate a focus on process improvement and be capable of articulating ideas for improving efficiency and maximizing results
  • Possess well-developed interpersonal skills and an ability to work well independently, as well as with co-workers, peers, supervisor and external customers
  • Able to maintain confidentiality with HIPAA guidelines, patient information and other sensitive information
  • Demonstrate professionalism, sense of urgency and self-motivation to achieve required metrics

Apply