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
$90 - $123/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)
San Diego, CA · On-site
$90 - $123/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)
Boston, MA · On-site
$2.5K/wk
Pharmacist Duration: 30 days Shift: 08:00 AM - 04:30 PM Hours per Shift: 8 hours Experience ... Your mobile info will not be shared with third parties for marketing. Standard messaging and data ...
Boston, MA · On-site
$2.5K/wk
Pharmacist Duration: 30 days Shift: 08:00 AM - 04:30 PM Hours per Shift: 8 hours Experience ... Your mobile info will not be shared with third parties for marketing. Standard messaging and data ...
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)
Bowling Green, KY · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research ... Corresponds directly with study sponsors to facilitate subject participation, submits subject visit ...
Bowling Green, KY · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research ... Corresponds directly with study sponsors to facilitate subject participation, submits subject visit ...
Washington, DC · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research ... Corresponds directly with study sponsors to facilitate subject participation, submits subject visit ...
Washington, DC · On-site
As clinical trials manager, responsibilities include review and mastery of clinical research ... Corresponds directly with study sponsors to facilitate subject participation, submits subject visit ...
Long Beach, CA · On-site
$23 - $30/hr
Assists with processing blood samples, urine samples, and/or pregnancy tests * Processes any trial ... Acts as back-up to the Clinical Trials Manager/Lead to answer any patient, sponsor, or physician ...
New
Long Beach, CA · On-site
$23 - $30/hr
Assists with processing blood samples, urine samples, and/or pregnancy tests * Processes any trial ... Acts as back-up to the Clinical Trials Manager/Lead to answer any patient, sponsor, or physician ...
New
Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing ... Experience interacting with clinical third parties (e.g., contract research organizations ...
Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing ... Experience interacting with clinical third parties (e.g., contract research organizations ...
Performs protocol-specific clinical tasks including patient assessment, ordering tests, collecting ... Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training within ...
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 ...
Director Clinical Trials Administration Job Category Management Schedule Full time Shift 1 - Day ... subject protection requirements, and institutional policies. Maintain research readiness for ...
Director Clinical Trials Administration Job Category Management Schedule Full time Shift 1 - Day ... subject protection requirements, and institutional policies. Maintain research readiness for ...
Atlanta, GA · On-site
$23.75 - $31.75/hr
Work Shift Day Work Day(s) Monday-Friday Shift Start Time 8:30 AM Shift End Time 5:00 PM Worker Sub ... Coordinates investigator-initiated and other clinical trials, including communication, regulatory ...
Atlanta, GA · On-site
$23.75 - $31.75/hr
Work Shift Day Work Day(s) Monday-Friday Shift Start Time 8:30 AM Shift End Time 5:00 PM Worker Sub ... Coordinates investigator-initiated and other clinical trials, including communication, regulatory ...
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 ...
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 ...
Akron, OH · On-site
$90 - $110/hr
... test new software releases. * 5. Creates and maintains system documentation, standard operating procedures (SOPs), work instructions, and training materials. * 6. Participates as a member of the ...
Akron, OH · On-site
$90 - $110/hr
... test new software releases. * 5. Creates and maintains system documentation, standard operating procedures (SOPs), work instructions, and training materials. * 6. Participates as a member of the ...
Vendor Management: • Oversee third-party vendors; reviews vendor reports, budgets, and metrics ... clinical trials are executed in compliance with international GCP guidelines/regulations and ...
Vendor Management: • Oversee third-party vendors; reviews vendor reports, budgets, and metrics ... clinical trials are executed in compliance with international GCP guidelines/regulations and ...
San Antonio, TX · On-site
Test new processes and systems for the management of data in clinical trials * Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and ...
San Antonio, TX · On-site
Test new processes and systems for the management of data in clinical trials * Test clinical trial databases and data entry screens assuring compliance with protocol and institutional processes and ...
Oklahoma City, OK · On-site
$55K - $72K/yr
Clinical Trials Manager - Oncore Data Job no: 493887 Work type: Managerial Location: Oklahoma City ... tests, and procedures. * High impact Contract Support - Support sponsor agreements and financial ...
Oklahoma City, OK · On-site
$55K - $72K/yr
Clinical Trials Manager - Oncore Data Job no: 493887 Work type: Managerial Location: Oklahoma City ... tests, and procedures. * High impact Contract Support - Support sponsor agreements and financial ...
... test new software releases. 5. Creates and maintains system documentation, standard operating ... Clinical Trials Management System Certification or Clinical Research certification (e.g. SOCRA ...
... test new software releases. 5. Creates and maintains system documentation, standard operating ... Clinical Trials Management System Certification or Clinical Research certification (e.g. SOCRA ...
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 ...
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Provide feedback on process improvements to DM Management and/or Subject Matter Experts (SMEs)
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... Provide feedback on process improvements to DM Management and/or Subject Matter Experts (SMEs)
$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
The most popular types of Clinical Trials Test Subject jobs are:

Full-time
Re-posted 28 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.