Extra Income Clinical Trial Participant

Care Health

Orem, UTPart-timePosted May 17, 2026

Behavioral Health Market Context

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Benefits

Financial recompense for engaging in tasksTravel expense coverage considerations to be aware ofParticipants may receive no-cost medical evaluations or health screenings as part of the study's benefitsMultiple ways to engage (participation flexibility, whether in-person or via remote access)

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:
• Comply with the directives from study coordinators and medical staff when engaging in clinical research studies
• Execute the study procedures, schedules, and guidelines meticulously
• Ensure your presence at the prescribed medical consultations, screenings, and subsequent follow-up appointments
• When needed, be sure to provide detailed health information and an accurate medical history
• Inform the study coordinators about any symptoms, adverse effects, or worries noted during the research process
• Participate in surveys, questionnaires, or health questionnaires associated with the study
• Follow the medication or treatment protocols as prescribed by the research team
• Comply with safety measures and ethical principles during the research project

Requirements:
• Ability to process and carry out instructions thoughtfully
• Interest in being involved in scientific studies conducted in the medical realm
• Conform to the study's eligibility specifications, which could involve age limitations, health status, and prior medical records
• Being able to participate in scheduled appointments or complete tasks that involve remote interaction
• Strong communication acumen and consistency are pivotal characteristics
• Experience in the medical field is not mandatory

Preferred Qualifications:
• Eagerness to play a role in furthering developments in the healthcare sector
• Skill in maintaining accurate personal health records
• Feeling relaxed about participating in medical evaluations or surveys

Compensation & Benefits:
• Financial recompense for engaging in tasks
• Travel expense coverage considerations to be aware of
• Participants may receive no-cost medical evaluations or health screenings as part of the study's benefits
• The opportunity to be a part of driving forward progress in medical research and scientific discoveries
• Multiple ways to engage (participation flexibility, whether in-person or via remote access)

Work Environment:

Clinical trials occur in hospitals, research centers, universities, or authorized medical facilities. Depending on the study requirements, remote participation may be permitted through online surveys or virtual monitoring.

Qualifications

  • Ability to process and carry out instructions thoughtfully
  • Interest in being involved in scientific studies conducted in the medical realm
  • Conform to the study's eligibility specifications, which could involve age limitations, health status, and prior medical records
  • Being able to participate in scheduled appointments or complete tasks that involve remote interaction
  • Strong communication acumen and consistency are pivotal characteristics
  • Experience in the medical field is not mandatory
  • The opportunity to be a part of driving forward progress in medical research and scientific discoveries
  • Depending on the study requirements, remote participation may be permitted through online surveys or virtual monitoring

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
  • Comply with the directives from study coordinators and medical staff when engaging in clinical research studies
  • Execute the study procedures, schedules, and guidelines meticulously
  • Ensure your presence at the prescribed medical consultations, screenings, and subsequent follow-up appointments
  • When needed, be sure to provide detailed health information and an accurate medical history
  • Inform the study coordinators about any symptoms, adverse effects, or worries noted during the research process
  • Participate in surveys, questionnaires, or health questionnaires associated with the study
  • Follow the medication or treatment protocols as prescribed by the research team
  • Comply with safety measures and ethical principles during the research project


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