Clinical Research Contributor

Care Health

Estero, FLPart-timePosted May 28, 2026

Behavioral Health Market Context

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Benefits

Payment for participating in tasksPotential repayment for incurred travel costsThe availability of complimentary health check-ups or medical evaluations is subject to the requirements of the studyThe potential to contribute to the growth and evolution of medical and scientific discoveries and practicesMultiple participation selections (choosing between in-person attendance or remote involvement, as per the trial's instructions)

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:
• Act in accordance with the guidelines established by study coordinators and healthcare providers during your participation in clinical research investigations
• Implement the study protocols, timetables, and procedures correctly
• Your presence is indispensable at the essential medical appointments, screenings, and follow-up visits
• It is essential to furnish accurate health information and a complete medical history when needed
• Report any symptoms, side effects, or concerns experienced while enrolled in the study to the relevant authorities
• Contribute to surveys, questionnaires, or health assessments in connection with the research
• Comply with the medication or treatment instructions issued by the research team
• Uphold safety protocols and ethical standards rigorously throughout the study

Requirements:
• Capability to grasp and adhere to instructions with care
• Eagerness to be part of studies and experiments in the realm of medical research
• Satisfy the study's distinct eligibility standards, involving criteria like age, health conditions, and past medical information
• Having the readiness to show up for scheduled meetings or complete tasks via remote interactions
• Excellent communication capabilities and reliability are highly valued
• Previous involvement in the medical field is not required

Preferred Qualifications:
• Drive to support and be part of the advancements occurring in healthcare
• Competence in sustaining accurate personal health records
• Having no reservations about joining in medical screenings or surveys

Compensation & Benefits:
• Payment for participating in tasks
• Potential repayment for incurred travel costs
• The availability of complimentary health check-ups or medical evaluations is subject to the requirements of the study
• The potential to contribute to the growth and evolution of medical and scientific discoveries and practices
• Multiple participation selections (choosing between in-person attendance or remote involvement, as per the trial's instructions)

Work Environment:

Clinical trials are carried out in different locations like hospitals, research centers, universities, or authorized medical facilities. Remote participation may be allowed in certain studies through the completion of online surveys or virtual monitoring, depending on the study specifications.

Qualifications

  • Capability to grasp and adhere to instructions with care
  • Eagerness to be part of studies and experiments in the realm of medical research
  • Satisfy the study's distinct eligibility standards, involving criteria like age, health conditions, and past medical information
  • Having the readiness to show up for scheduled meetings or complete tasks via remote interactions
  • Excellent communication capabilities and reliability are highly valued
  • Previous involvement in the medical field is not required
  • Remote participation may be allowed in certain studies through the completion of online surveys or virtual monitoring, depending on the study specifications

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
  • Act in accordance with the guidelines established by study coordinators and healthcare providers during your participation in clinical research investigations
  • Implement the study protocols, timetables, and procedures correctly
  • Your presence is indispensable at the essential medical appointments, screenings, and follow-up visits
  • It is essential to furnish accurate health information and a complete medical history when needed
  • Report any symptoms, side effects, or concerns experienced while enrolled in the study to the relevant authorities
  • Contribute to surveys, questionnaires, or health assessments in connection with the research
  • Comply with the medication or treatment instructions issued by the research team
  • Uphold safety protocols and ethical standards rigorously throughout the study


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