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Temporary Clinical Trials Test Subject Jobs in Boca Raton, FL

Segal Trials

Clinical Research Coordinator

Lauderhill, FL · On-site

$24 - $32/hr

... subject and family members regarding specific studies and clinical drug trials in general. · Complete all monitor and sponsor queries in a timely manner. · Perform some phlebotomy · Perform ...

Segal Trials

Clinical Research Coordinator

Hollywood, FL · On-site

$22.25 - $29.50/hr

... subject and family members regarding specific studies and clinical drug trials in general. · Complete all monitor and sponsor queries in a timely manner. · Perform some phlebotomy · Perform ...

Segal Trials

Clinical Rater

Boynton Beach, FL · On-site

... subject's current presentation throughout the duration of the trials. Clinical interviewing skills are a must, as well as knowledge of DSM IV and 5 diagnoses. DUTIES & ESSENTIAL JOB FUNCTIONS · ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

Coordinate all aspects of assigned clinical trials from site initiation to study close-out * Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards * Maintain ...

VENTRE MEDICAL ASSOCIATES

Rater

Fort Lauderdale, FL · On-site

$23 - $30.75/hr

Become familiar with the FDA Regulations pertaining to clinical trials * Perform interview/ratings ... Complete subject eligibility/screening forms, as necessary and fax/email to study team, as ...

RESEARCH CENTERS OF AMERICA GROUP

Rater

Fort Lauderdale, FL · On-site

$23 - $30.75/hr

Become familiar with the FDA Regulations pertaining to clinical trials * Perform interview/ratings ... Complete subject eligibility/screening forms, as necessary and fax/email to study team, as ...

CenExel

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Responsible for performing various clinical and neurocognitive test evaluations and interview ...

CenExel

Clinical Rater

Hollywood, FL · On-site

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Responsible for performing various clinical and neurocognitive test evaluations and interview ...

Headlands Research

Clinical Research Coordinator

Lake Worth, FL · On-site

$21.50 - $28.75/hr

Coordinate all aspects of assigned clinical trials from site initiation to study close-out * Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards * Maintain ...

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All JobsClinical Trials Test Subject JobsTemporary Clinical Trials Test Subject JobsTemporary Clinical Trials Test Subject Jobs in Boca Raton, FL

Temporary Clinical Trials Test Subject information

See Boca Raton, FL salary details

$15

$51

$85

How much do temporary clinical trials test subject jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for temporary clinical trials test subject in Boca Raton, FL is $51.41, according to ZipRecruiter salary data. Most workers in this role earn between $32.64 and $77.31 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Trials Test Subject vs Clinical Research Coordinator?

AspectTemporary Clinical Trials Test SubjectClinical Research Coordinator
CredentialsNo formal certifications typically required; must meet trial-specific criteriaUsually requires a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentParticipates in clinical trials, often in medical facilities or research centersWorks in research sites, hospitals, or clinics managing trial operations
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding trial participation rolesManaging and coordinating clinical trials

The main difference is that Temporary Clinical Trials Test Subjects participate in trials without requiring extensive certifications, focusing on trial participation. Clinical Research Coordinators, however, manage and oversee the trial process, often needing relevant certifications and experience. Both roles are essential in clinical research but serve different functions within the industry.

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For Temporary Clinical Trials Test Subject jobs in Boca Raton, FL, the most frequently searched job titles are:

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Temporary Clinical Trials Test Subject jobs near you

Principal Investigator (MD/DO) - Respiratory Clinical Trials

Hawthorne Health

Boynton Beach, FL

$150 - $250/hr

Contractor

Posted 11 days ago

Job description

About Us 
Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster. 
 
About the Role
Hawthorne Health is seeking an experienced Principal investigator (MD/DO) for a part-time, 1099 role. Candidates should have prior experience as a PI or Sub-I on sponsor-initiated clinical trials. This role will lead Respiratory trials including Asthma within our growing, community-based site network—built to make research efficient, patient-friendly, and investigator-supported.
Responsibilities
  • Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable.
  • Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
  • Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff.
  • Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight.
  • Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment.
  • Review and interpret laboratory results, ECGs, and other diagnostic tests.
  • Make critical medical decisions regarding participant care, adverse events, and protocol deviations.
  • Ensure accurate, complete, and timely collection and documentation of all study data.
  • Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
  • Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team.
  • Participate in site initiation visits, monitoring visits, audits, and inspections.
  • Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas.
Requirements
  • Must be an MD with experience leading at least three sponsor initiated trials as a PI or Sub-I.
  • Current, unrestricted medical license.
  • Experience with respiratory indications in clinical trials and/or in a clinical setting.
  • Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
  • Proven leadership and team management skills.
  • Excellent clinical judgment and decision-making abilities.
  • Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely.
  • Exceptional organizational skills and meticulous attention to detail.
  • Ability to manage multiple complex studies simultaneously and prioritize tasks effectively.
  • Commitment to ethical conduct and patient safety.
Location
  • This role requires on-site presence approximately twice per month for key visits (or more, depending on study needs), with additional oversight responsibilities performed remotely (approximately 3–5 hours per week).
  • Preference is for Investigator to live within 1.5 hours driving distance of the site. 
This is a 1099 independent contractor opportunity. Compensation may be flexible and adjusted based on experience and qualifications.

Hawthorne Health is transforming the clinical trial landscape through an innovative site model that integrates research into community-based settings like local pharmacies. By meeting patients where they already receive care, we are improving access, strengthening trust, and driving more inclusive and efficient trials.

We welcome the opportunity to connect with individuals interested in being part of this evolving model.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/Terms of Use: https://hawthornehealth.com/terms-of-use/