Clinical Research for Extra Cash

Care Health

Ithaca, NYPart-timePosted Jun 11, 2026

Behavioral Health Market Context

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Benefits

Monetary reward for involvementOptions for reimbursement of travel costsFree access to health check-ups or medical assessments may be available depending on the specific research projectThe possibility of making valuable contributions to the fields of medicine and science through active engagementDiverse participation alternatives (attending in person or joining remotely, as the trial dictates)

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:
• Adhere to the instructions given by study coordinators and healthcare professionals during your participation in clinical research projects
• Adhere meticulously to the study guidelines, schedules, and procedures
• It is important to attend all mandatory medical appointments, screenings, and subsequent check-ups
• Accurate health information and a detailed medical history should be provided when requested
• Report any signs, impacts, or issues encountered while participating in the research
• Engage in surveys, questionnaires, or health appraisals relevant to the research
• Comply with the medication or treatment directives provided by the research team
• Adhere to safety protocols and ethical standards without deviation during the study

Requirements:
• Facility in understanding and obeying directives with accuracy
• Readiness to partake in studies within the medical research field
• Meet the study's designated eligibility criteria, which may include age restrictions, health conditions, and individual medical profiles
• The capacity to attend set appointments or fulfill tasks requiring remote involvement
• Effective communication prowess and reliability are essential traits
• Previous healthcare knowledge is not a prerequisite

Preferred Qualifications:
• Inclination towards making a meaningful impact on healthcare advancements
• Capacity to retain precise personal health information
• Being comfortable when engaging in health assessments or research questionnaires

Compensation & Benefits:
• Monetary reward for involvement
• Options for reimbursement of travel costs
• Free access to health check-ups or medical assessments may be available depending on the specific research project
• The possibility of making valuable contributions to the fields of medicine and science through active engagement
• Diverse participation alternatives (attending in person or joining remotely, as the trial dictates)

Work Environment:

Clinical trials can be conducted in hospitals, research centers, universities, or approved medical facilities. Depending on the study requirements, some trials may offer remote participation through online surveys or virtual monitoring.

Qualifications

  • Facility in understanding and obeying directives with accuracy
  • Meet the study's designated eligibility criteria, which may include age restrictions, health conditions, and individual medical profiles
  • The capacity to attend set appointments or fulfill tasks requiring remote involvement
  • Effective communication prowess and reliability are essential traits
  • Previous healthcare knowledge is not a prerequisite
  • Depending on the study requirements, some trials may offer remote participation 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
  • Adhere to the instructions given by study coordinators and healthcare professionals during your participation in clinical research projects
  • Adhere meticulously to the study guidelines, schedules, and procedures
  • It is important to attend all mandatory medical appointments, screenings, and subsequent check-ups
  • Accurate health information and a detailed medical history should be provided when requested
  • Report any signs, impacts, or issues encountered while participating in the research
  • Engage in surveys, questionnaires, or health appraisals relevant to the research
  • Comply with the medication or treatment directives provided by the research team
  • Adhere to safety protocols and ethical standards without deviation during the study
  • Readiness to partake in studies within the medical research field


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