Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and management methodologies of clinical trial. * Ability to demonstrate ...
Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and management methodologies of clinical trial. * Ability to demonstrate ...
Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and management methodologies of clinical trial. * Ability to demonstrate ...
Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and management methodologies of clinical trial. * Ability to demonstrate ...
Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...
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Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...
Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...
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Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Job Title: Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a ...
Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a dedicated clinical ...
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Clinical Trials Recruiter
Brooklyn, NY · On-site +1
$20 - $30/hr
Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on experience Job Type: [Part-time but potential to become full-time]. About Us We are a dedicated clinical ...
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Clinical Trials Manager
Wilmington, DE · On-site
The Clinical Trials Manager provides strategic planning, growth, and development for Clinical Research conducted in the Delaware Valley. The incumbent supervises and coordinates the responsibilities ...
Conventional clinical trials, community and population health, social, behavioral, and educational research. Community education, well-defined research initiation process, ongoing and continued ...
Conventional clinical trials, community and population health, social, behavioral, and educational research. Community education, well-defined research initiation process, ongoing and continued ...
The Clinical Trials Office Director reports to the Vice President for Research at MaineHealth. The Director is responsible for the development, promotion, and leadership of the Clinical Trials Office ...
The Clinical Trials Office Director reports to the Vice President for Research at MaineHealth. The Director is responsible for the development, promotion, and leadership of the Clinical Trials Office ...
In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
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Clinical Trials Operations Specialist
Irvine, CA · On-site
$30 - $35/hr
The Clinical Trials Operations Specialist would be working for a Fortune 500 Biomedical company. If interested APPLY NOW for IMMEDIATE consideration!! Clinical Trials Operations Specialist Job ...
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Be Seen First
Clinical Trials Operations Specialist
Irvine, CA · On-site
$30 - $35/hr
The Clinical Trials Operations Specialist would be working for a Fortune 500 Biomedical company. If interested APPLY NOW for IMMEDIATE consideration!! Clinical Trials Operations Specialist Job ...
Clinical Trials Specialist (2 Openings)
New Brunswick, NJ · On-site
$81K/yr
The Clinical Trials Specialist (CTS) serves as the chief contact for all new research patient referrals. The Clinical Trials Specialist will work with members of the clinical research team to ...
Clinical Trials Specialist (2 Openings)
New Brunswick, NJ · On-site
$81K/yr
The Clinical Trials Specialist (CTS) serves as the chief contact for all new research patient referrals. The Clinical Trials Specialist will work with members of the clinical research team to ...
Clinical Research Certification with ACRP or SoCRA Qualifications * Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and ...
Clinical Research Certification with ACRP or SoCRA Qualifications * Knowledge of scientific concepts related to the design and analysis of clinical trials. * Knowledge of data collection and ...
Coordinates, evaluates, and follows patients in clinical trials, which includes but is not limited to screening, identifying, enrolling and consenting patients, developing study calendars with ...
Coordinates, evaluates, and follows patients in clinical trials, which includes but is not limited to screening, identifying, enrolling and consenting patients, developing study calendars with ...
Clinical Trials Coordinator (1272)
Leesburg, FL · On-site
$19.78/hr
The Clinical Trials Coordinator at LIFESTREAM BEHAVIORAL CENTER will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ensuring that all ...
Clinical Trials Coordinator (1272)
Leesburg, FL · On-site
$19.78/hr
The Clinical Trials Coordinator at LIFESTREAM BEHAVIORAL CENTER will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ensuring that all ...
Job Purpose: - The Clinical Trials Coordinator at LIFESTREAM BEHAVIORAL CENTER will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ...
Job Purpose: - The Clinical Trials Coordinator at LIFESTREAM BEHAVIORAL CENTER will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ...
Working in a GxP environment. experience with clinical outsourcing, clinical trials required for this role. understanding life cycle of clinical trials Understand the Marketplace and Category of ...
Working in a GxP environment. experience with clinical outsourcing, clinical trials required for this role. understanding life cycle of clinical trials Understand the Marketplace and Category of ...
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
CTM may lead the cross-functional CTT for smaller and less complex trials or manage critical aspects of larger and more complex clinical trials under CTL leadership. In addition, CTM will be ...
Clinical Trials Manager
Chicago, IL · On-site +1
The Alliance for Clinical Trials in Oncology at the University of Chicago serves as the office for scientific protocol, administrative, regulatory and pharmaceutical affairs operations of the ...
Clinical Trials Manager
Chicago, IL · On-site +1
The Alliance for Clinical Trials in Oncology at the University of Chicago serves as the office for scientific protocol, administrative, regulatory and pharmaceutical affairs operations of the ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high ...
Clinical Trials Manager
Foster City, CA · On-site
Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high ...
Clinical Trials information
See salary details
$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
How much do clinical trials jobs pay per hour?
What are the key skills and qualifications needed to thrive in the Clinical Trials position, and why are they important?
To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.
What are some common career paths or advancement opportunities for professionals working in Clinical Trials?
Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.
What is a Clinical Trials job?
A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

UT Health San Antonio rating
7.7
Based on 40 frontline employees who took The Breakroom Quiz
215th of 535 rated colleges and universities
Job description
- Knowledge of scientific concepts related to the design and analysis of clinical trials.
- Knowledge of data collection and management methodologies of clinical trial.
- Ability to demonstrate excellent written and verbal communication.
- Proficiency with computers, including Microsoft Office.
EDUCATION:
Bachelor's Degree degree in related field is required.
PREFERRED:
IRB experience, regulatory affairs experience, and clinical trials experience
This position may require the ability to maintain the security and integrity of UT San Antonio and its infrastructure per Texas EO-GA-48.
- Administers, organizes and conducts training/educational programs in connection with clinical trial operations, systems and management.
- Maintains records of training activities, progress, and program effectiveness.
- Ensures distribution and maintains inventory required for execution of research protocol(s).
- Assists in the determination of guidelines for new protocols.
- Collects and prepares data for various clinical trial related reports.
- Compiles reports, documents and correspondence for regulatory agencies, participating clinical trial sites and internal departments to monitor and evaluate progress.
- Develops, coordinates and conducts training in collaboration with clinical trial subject matter experts.
- Serves as liaison between clinical trial management systems end users and management systems support team.
- Performs all other duties as assigned.
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About UT Health San Antonio
Sourced by ZipRecruiter
Industry
Colleges, universities, and professional schools
Company size
5,001 - 10,000 Employees
Headquarters location
San Antonio, TX, US
Year founded
1959