Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Performs subject recruitment, screening, consenting, coordination of clinical visits/protocol ... Our clinical trials program is dedicated to bringing cutting-edge advances in treatments to our ...
Performs subject recruitment, screening, consenting, coordination of clinical visits/protocol ... Our clinical trials program is dedicated to bringing cutting-edge advances in treatments to our ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Performs subject recruitment, screening, consenting, coordination of clinical visits/protocol ... Our clinical trials program is dedicated to bringing cutting-edge advances in treatments to our ...
Performs subject recruitment, screening, consenting, coordination of clinical visits/protocol ... Our clinical trials program is dedicated to bringing cutting-edge advances in treatments to our ...
Clinical Trials Project Manager
Los Angeles, CA · On-site
$31.51 - $62.64/hr
... Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO-US ... Current/former UC employees are subject to a personnel file review.
Clinical Trials Project Manager
Los Angeles, CA · On-site
$31.51 - $62.64/hr
... Clinical Trials Development (CTD) supports clinical research efforts at UCLA and within the TRIO-US ... Current/former UC employees are subject to a personnel file review.
RN CLINICAL TRIALS
Lansing, MI · On-site
... tests, releasing chemotherapy, Lab tests and ECG reports to ensure compliance with protocols ... clinical trials. • Experience with computer data entry and database management • Excellence ...
New
RN CLINICAL TRIALS
Lansing, MI · On-site
... tests, releasing chemotherapy, Lab tests and ECG reports to ensure compliance with protocols ... clinical trials. • Experience with computer data entry and database management • Excellence ...
New
Physician - Clinical Trials - MD/DO Albuquerque, New Mexico At Headlands Research, we are dedicated ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO Albuquerque, New Mexico At Headlands Research, we are dedicated ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO At Headlands Research, we are dedicated to enhancing clinical ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO At Headlands Research, we are dedicated to enhancing clinical ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO Little Rock, AR At Headlands Research, we are dedicated to ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO Little Rock, AR At Headlands Research, we are dedicated to ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Associate Specialist, Clinical Trials
San Diego, CA · On-site
$101.29/hr
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate data ... subject safety and impeccable documentation. Your Contributions (include, but are not limited to)
Associate Specialist, Clinical Trials
San Diego, CA · On-site
$101.29/hr
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate data ... subject safety and impeccable documentation. Your Contributions (include, but are not limited to)
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us-it's central to our ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
... of subject participation and procedures as required by protocol. * Obtains informed consent ... Selects, applies and tests standard methodologies, techniques and tools such as manuals, forms and ...
... of subject participation and procedures as required by protocol. * Obtains informed consent ... Selects, applies and tests standard methodologies, techniques and tools such as manuals, forms and ...
Experience coordinating clinical trials in Oncology. Knowledge of the IRB/regulatory process. IRB ... Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and ...
Experience coordinating clinical trials in Oncology. Knowledge of the IRB/regulatory process. IRB ... Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and ...
... subject screening, informed consent, data entry, regulatory compliance, and coordination with ... Coordinate and conduct clinical trials according to GCP, ICH, FDA, and sponsor guidelines.
Quick apply
... subject screening, informed consent, data entry, regulatory compliance, and coordination with ... Coordinate and conduct clinical trials according to GCP, ICH, FDA, and sponsor guidelines.
CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr
Recruit and screen subjects for clinical trials and maintain all logs * Orient research subjects to ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
Quick apply
CLINICAL RESEARCH COORDINATOR
Miami, FL · On-site
$40K - $55K/yr
Recruit and screen subjects for clinical trials and maintain all logs * Orient research subjects to ... Collect, Record and maintain research subject study data according to protocol and SOPS * Handle ...
Physician - Clinical Trials - MD/DO At Headlands Research, we are dedicated to enhancing clinical ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
Physician - Clinical Trials - MD/DO At Headlands Research, we are dedicated to enhancing clinical ... Oversee subject safety, trial conduct compliance, and the informed consent process. * Communicate ...
... of subject participation and procedures as required by protocol. * Obtains informed consent ... Selects, applies and tests standard methodologies, techniques and tools such as manuals, forms and ...
... of subject participation and procedures as required by protocol. * Obtains informed consent ... Selects, applies and tests standard methodologies, techniques and tools such as manuals, forms and ...
Temporary Clinical Trials Test Subject information
See salary details
$16.35 - $23.03
8% of jobs
$23.03 - $29.72
0% of jobs
$33.41 is the 25th percentile. Wages below this are outliers.
$29.72 - $36.41
30% of jobs
The median wage is $41.66 / hr.
$36.41 - $43.09
15% of jobs
$43.09 - $49.78
8% of jobs
$49.78 - $56.47
1% of jobs
$56.47 - $63.16
0% of jobs
$63.16 - $69.84
8% of jobs
$69.84 - $76.53
1% of jobs
$78.76 is the 75th percentile. Wages above this are outliers.
$76.53 - $83.22
9% of jobs
$83.22 - $89.90
19% of jobs
$16
$54
$89
How much do temporary clinical trials test subject jobs pay per hour?
What is the difference between Temporary Clinical Trials Test Subject vs Clinical Research Coordinator?
| Aspect | Temporary Clinical Trials Test Subject | Clinical Research Coordinator |
|---|---|---|
| Credentials | No formal certifications typically required; must meet trial-specific criteria | Usually requires a bachelor's degree in health sciences or related field; certifications like CCRP are common |
| Work Environment | Participates in clinical trials, often in medical facilities or research centers | Works in research sites, hospitals, or clinics managing trial operations |
| Employer & Industry | Pharmaceutical companies, research organizations, hospitals | Research institutions, hospitals, pharmaceutical companies |
| Search & Comparison Intent | Understanding trial participation roles | Managing 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.
What cities are hiring for Temporary Clinical Trials Test Subject jobs?
Cities with the most Temporary Clinical Trials Test Subject job openings:
What are the most commonly searched types of Clinical Trials Test Subject jobs?
The most popular types of Clinical Trials Test Subject jobs are:
What states have the most Temporary Clinical Trials Test Subject jobs?
States with the most job openings for Temporary Clinical Trials Test Subject jobs include:
What job categories do people searching Temporary Clinical Trials Test Subject jobs look for?
The top searched job categories for Temporary Clinical Trials Test Subject jobs are:

Physician - Clinical Trials - MD/DO
Las Cruces, NM • On-site
Full-time, Part-time
Re-posted 10 days ago
Job description
Join Us in Improving Lives through Clinical Research
At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.
Championing Diversity in Clinical Trials
Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.
The Role of a Lifetime
Are you ready to make a difference? We're seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Las Cruces area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible-we're open to part-time or full-time commitments with flexible schedules.
Why Join Us?
- Flexible Schedule: Work on your terms, with a schedule that fits your life.
- Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
- Dynamic Team Environment: You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.
Responsibilities:
- Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
- Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
- Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
- Obtain IRB approval for study initiation and any protocol modifications.
- Oversee subject safety, trial conduct compliance, and the informed consent process.
- Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
- Provide ongoing training and support to research staff.
Requirements:
- Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
- Active and unencumbered license to practice as an MD or DO within the state of New Mexico required.
- Must be board-certified or board-eligible.
- Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
- Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
- Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.
About Headlands Research
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
Lake Worth, FL, US