HCT is seeking an interim Clinical Trials Subject Matter Expert for a 240+ bed hospital in California. The responsibilities include: * With direction from the PI, this position coordinates research ...
Quick apply
HCT is seeking an interim Clinical Trials Subject Matter Expert for a 240+ bed hospital in California. The responsibilities include: * With direction from the PI, this position coordinates research ...
Quick apply
HCT is seeking an interim Clinical Trials Subject Matter Expert for a 240+ bed hospital in California. The responsibilities include: * With direction from the PI, this position coordinates research ...
San Diego, CA · On-site
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate data ... subject safety and impeccable documentation. Your Contributions (include, but are not limited to)
San Diego, CA · On-site
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate data ... subject safety and impeccable documentation. Your Contributions (include, but are not limited to)
Honolulu, HI · On-site
Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting ... Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within ...
Honolulu, HI · On-site
Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting ... Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within ...
Honolulu, HI · On-site
$125K - $130K/yr
Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting ... Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within ...
Honolulu, HI · On-site
$125K - $130K/yr
Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting ... Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within ...
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate ... data, subject safety and impeccable documentation. _ Your Contributions (include, but are not ...
... trials adhering to Good Clinical Practice (GCP) and ensuring accurate ... data, subject safety and impeccable documentation. _ Your Contributions (include, but are not ...
Miami, FL · On-site
$40.40 - $53.73/hr
The Clinical Trials Nurse effectively conducts assigned operations of research protocols ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
Miami, FL · On-site
$40.40 - $53.73/hr
The Clinical Trials Nurse effectively conducts assigned operations of research protocols ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
Miami, FL · On-site
$40.40 - $53.73/hr
... trials ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
Miami, FL · On-site
$40.40 - $53.73/hr
... trials ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
Boston, MA · On-site
$2.5K/wk
The Clinical Trials Pharmacy offers pharmaceutical services and guidance to support research groups and investigators engaged in the conduct of human subject research. * The unit is dedicated to the ...
New
Boston, MA · On-site
$2.5K/wk
The Clinical Trials Pharmacy offers pharmaceutical services and guidance to support research groups and investigators engaged in the conduct of human subject research. * The unit is dedicated to the ...
New
... service, subject-facing clinical research support to investigators across the institution ... Develop and manage the Clinical Trials Unit operating budget, demonstrating sound financial ...
... service, subject-facing clinical research support to investigators across the institution ... Develop and manage the Clinical Trials Unit operating budget, demonstrating sound financial ...
Miami, FL · On-site
$40.40 - $53.73/hr
... trials ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
Miami, FL · On-site
$40.40 - $53.73/hr
... trials ... Performs protocol specific clinical tasks including patient assessment, screening, ordering tests ...
... test new software releases. 5. Creates and maintains system documentation, standard operating ... Clinical Trials Management System Certification or Clinical Research certification (e.g. SOCRA ...
New
... test new software releases. 5. Creates and maintains system documentation, standard operating ... Clinical Trials Management System Certification or Clinical Research certification (e.g. SOCRA ...
New
... subject protection requirements, and institutional policies. Maintain research readiness for ... or clinical trials operations. * Three (3) years of leadership experience managing research ...
... subject protection requirements, and institutional policies. Maintain research readiness for ... or clinical trials operations. * Three (3) years of leadership experience managing research ...
Tucson, AZ · On-site
$120 - $160/hr
Ensure compliance with FDA regulations, ICH Good Clinical Practice, HIPAA, human subject protection ... trials operations. * Three (3) years of leadership experience managing research personnel and ...
Tucson, AZ · On-site
$120 - $160/hr
Ensure compliance with FDA regulations, ICH Good Clinical Practice, HIPAA, human subject protection ... trials operations. * Three (3) years of leadership experience managing research personnel and ...
OR · On-site +1
This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.
OR · On-site +1
This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.
Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials.
Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials.
Position Summary At Stony Brook Medicine, the Cancer Clinical Trials Finance Manager will manage ... All Hospital positions maybe subject to changes in pass days and shifts as necessary. * This ...
Position Summary At Stony Brook Medicine, the Cancer Clinical Trials Finance Manager will manage ... All Hospital positions maybe subject to changes in pass days and shifts as necessary. * This ...
Boston, MA · Hybrid
$77K - $102K/yr
The CRM will oversee the subject enrollment, protocol treatment and follow-up care processes for ... trials start-up, active and close out phases, clinical research local policy and federal regulation.
New
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Boston, MA · Hybrid
$77K - $102K/yr
The CRM will oversee the subject enrollment, protocol treatment and follow-up care processes for ... trials start-up, active and close out phases, clinical research local policy and federal regulation.
New
Assists with the informed consent process and ensures that the patient/subject fully understands ... This may include abstraction of data from the patient chart (e.g., laboratory or diagnostic test ...
Assists with the informed consent process and ensures that the patient/subject fully understands ... This may include abstraction of data from the patient chart (e.g., laboratory or diagnostic test ...
Coordinate and schedule subject visits within study/subject specific windows per protocol ... years of clinical trials research assistant experience in a retina or general ophthalmology ...
Quick apply
Coordinate and schedule subject visits within study/subject specific windows per protocol ... years of clinical trials research assistant experience in a retina or general ophthalmology ...
Coordinate and schedule subject visits within study/subject specific windows per protocol ... years of clinical trials research assistant experience in a retina or general ophthalmology ...
Coordinate and schedule subject visits within study/subject specific windows per protocol ... years of clinical trials research assistant experience in a retina or general ophthalmology ...
$28.85 - $34.97
4% of jobs
$34.97 - $41.08
6% of jobs
$41.08 - $47.20
7% of jobs
$51.79 is the 25th percentile. Wages below this are outliers.
$47.20 - $53.32
9% of jobs
$53.32 - $59.44
15% of jobs
The median wage is $62.14 / hr.
$59.44 - $65.56
18% of jobs
$69.92 is the 75th percentile. Wages above this are outliers.
$65.56 - $71.68
21% of jobs
$71.68 - $77.80
7% of jobs
$77.80 - $83.92
6% of jobs
$83.92 - $90.03
3% of jobs
$90.03 - $96.15
2% of jobs
$28
$62
$96
A Clinical Trials Test Subject participates in medical research studies to help test the safety and effectiveness of new treatments, medications, or medical devices. Subjects may undergo various tests, treatments, or monitoring under the supervision of healthcare professionals. Participation is voluntary, and subjects are informed of potential risks and benefits before enrolling. Compensation, requirements, and study duration vary depending on the trial.
As a Clinical Trials Test Subject, your day may involve undergoing scheduled medical tests, taking investigational medication or using new devices, and closely following instructions provided by research staff. You might spend time at a research facility for monitoring or complete tasks at home such as logging symptoms or side effects in an electronic diary. Interactions with clinical coordinators and regular health check-ins are common, ensuring your safety and accurate data collection. The environment is typically supportive, structured, and geared toward maintaining participant comfort and well-being throughout the study.
To thrive as a Clinical Trials Test Subject, you need to meet specific health and demographic criteria, have reliable transportation, and be willing to follow detailed study protocols. Familiarity with basic health assessments and the ability to use electronic diaries or monitoring devices are sometimes required. Dependability, attention to detail, and clear communication with research staff are valuable soft skills in this role. These qualities ensure the accuracy of trial data, participant safety, and smooth execution of clinical research studies.
Cities with the most Clinical Trials Test Subject job openings:
The most popular types of Clinical Trials Test Subject jobs are:
States with the most job openings for Clinical Trials Test Subject jobs include:
The top searched job categories for Clinical Trials Test Subject jobs are:

Full-time
Re-posted 12 days ago
HCT is seeking an interim Clinical Trials Subject Matter Expert for a 240+ bed hospital in California.
The responsibilities include:
Requirements:
Expenses are covered while on assignment including housing, airfare, and rental car.
Earn $2,000 for every candidate or position placement from your referral that HCT successfully places! Submit Referral Here
Keywords: Subject Matter Expert (SME), Clinical Trial Subject Matter Expert, Clinical Research Consultant, Clinical Research Manager, Clinical Trial Manager (CTM), Senior Clinical Trial Manager, Clinical Operations Manager, Director of Clinical Operations, Associate Director of Clinical Operations, Clinical Program Manager, Clinical Project Manager, Clinical Development Manager, Clinical Research Scientist, Clinical Scientist, Medical Affairs Manager, Research Nurse, Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Principal CRA, Clinical Trial Lead, Clinical Trials, Clinical Research, Clinical Operations, Phase I, Phase II, Phase III, Phase IV, Investigator-Initiated Trials (IIT), Multicenter Studies, Global Clinical Trials, Site Management, Trial Startup, Study Start-Up, Patient Recruitment, Site Activation, Clinical Monitoring.