Flexible Schedule Paid Health Study

Care Health

South Ogden, UTPart-timePosted Jun 11, 2026

Behavioral Health Market Context

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Benefits

Payment for taking part in activitiesReimbursement possibilities for travel-related expendituresDepending on the study, participants may qualify for complimentary health assessments or medical screeningsThe chance to actively engage in the improvement and development of medical and scientific innovationsVarious choices for engagement (in-person or virtual learning, based on the specific study)

Job Description

Job Summary:

A Paid Clinical Trials Participant volunteers to take part in medical research studies designed to evaluate new medications, treatments, medical devices, or healthcare procedures. Participants contribute to the advancement of medical knowledge while receiving compensation for their time, travel, and involvement. Clinical trials are conducted in controlled environments under the supervision of licensed healthcare professionals to ensure participant safety and study accuracy.

Key Responsibilities:
• Follow the guidance provided by study coordinators and medical professionals when taking part in clinical research trials
• Comply accurately with the study guidelines, schedules, and protocols
• Make sure to be present at the necessary medical appointments, screenings, and follow-up visits as instructed
• Provide thorough health information and a comprehensive medical history as and when required
• Notify the researchers of any indications, adverse reactions, or anxieties experienced throughout the examination
• Take surveys, questionnaires, or health inventories related to the research
• Adhere to the medication or treatment guidance given by the research group
• Conform to safety protocols and ethical standards throughout the study duration

Requirements:
• Talent for comprehending and adhering to instructions closely
• The inclination to engage in medical research investigations
• Abide by the study's unique eligibility criteria, which can encompass age requirements, health conditions, and medical history
• Having the capability to make it to arranged appointments or fulfill obligations for remote participation
• Reliable communication skills and dependability are indispensable qualities
• Medical background is not necessary

Preferred Qualifications:
• A desire to participate in the progress of healthcare innovations
• Capability to uphold exact personal health information
• Feeling at ease with taking part in medical screenings or questionnaires

Compensation & Benefits:
• Payment for taking part in activities
• Reimbursement possibilities for travel-related expenditures
• Depending on the study, participants may qualify for complimentary health assessments or medical screenings
• The chance to actively engage in the improvement and development of medical and scientific innovations
• Various choices for engagement (in-person or virtual learning, based on the specific study)

Work Environment:

Clinical trials take place in hospitals, research centers, universities, or approved medical facilities. Remote participation through online surveys or virtual monitoring may be available in some studies, depending on the study requirements.

Qualifications

  • Talent for comprehending and adhering to instructions closely
  • The inclination to engage in medical research investigations
  • Abide by the study's unique eligibility criteria, which can encompass age requirements, health conditions, and medical history
  • Having the capability to make it to arranged appointments or fulfill obligations for remote participation
  • Reliable communication skills and dependability are indispensable qualities
  • Medical background is not necessary
  • Remote participation through online surveys or virtual monitoring may be available in some studies, depending on the study requirements

Responsibilities

  • A Paid Clinical Trials Participant volunteers to take part in medical research studies designed to evaluate new medications, treatments, medical devices, or healthcare procedures
  • Participants contribute to the advancement of medical knowledge while receiving compensation for their time, travel, and involvement
  • Clinical trials are conducted in controlled environments under the supervision of licensed healthcare professionals to ensure participant safety and study accuracy
  • Follow the guidance provided by study coordinators and medical professionals when taking part in clinical research trials
  • Comply accurately with the study guidelines, schedules, and protocols
  • Make sure to be present at the necessary medical appointments, screenings, and follow-up visits as instructed
  • Provide thorough health information and a comprehensive medical history as and when required
  • Notify the researchers of any indications, adverse reactions, or anxieties experienced throughout the examination
  • Take surveys, questionnaires, or health inventories related to the research
  • Adhere to the medication or treatment guidance given by the research group
  • Conform to safety protocols and ethical standards throughout the study duration


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