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 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 ...
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 ...
Clinical Trials Manager
Foster City, CA · On-site
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.
Clinical Trials Manager
Foster City, CA · On-site
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.
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 ...
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 ...
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
Boston, MA · On-site
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
Boston, MA · On-site
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 ...
The Project Mganager, Clinical Trials develops and implements comprehensive workflows and project ... weekend shifts. In addition to our compensation for full-time and part-time (20+ hours/week) job ...
The Project Mganager, Clinical Trials develops and implements comprehensive workflows and project ... weekend shifts. In addition to our compensation for full-time and part-time (20+ hours/week) job ...
Qualifications Clinical SOP experience Clinical trials software MS Office 6+ YEARS experience actually working on a clinical trial team and/or experience writing clinical trial SOPs and associated ...
Qualifications Clinical SOP experience Clinical trials software MS Office 6+ YEARS experience actually working on a clinical trial team and/or experience writing clinical trial SOPs and associated ...
Weekend 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 weekend clinical trials jobs pay per hour?
As of Jun 9, 2026, the average hourly pay for weekend clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.
What is the difference between Weekend Clinical Trials vs Part-Time Clinical Research Coordinator?
| Aspect | Weekend Clinical Trials | Part-Time Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires clinical trial experience, basic medical knowledge | Requires certification in clinical research or related field, experience preferred |
| Work Environment | Conducted at research sites, hospitals, or clinics during weekends | Office-based, overseeing trial activities, often flexible hours |
| Employer & Industry | Pharmaceutical companies, research organizations, hospitals | Research institutions, hospitals, clinical trial sites |
| Search & Comparison Intent | Understanding weekend trial roles, flexible clinical trial work | Part-time research coordination, clinical trial management |
Weekend Clinical Trials involve participating in or managing clinical studies during weekends, often at research sites. Part-Time Clinical Research Coordinators oversee trial activities, ensuring compliance and data collection, usually during regular hours but on a part-time basis. Both roles support clinical research but differ in schedule, responsibilities, and required credentials.
What cities are hiring for Weekend Clinical Trials jobs? Cities with the most Weekend Clinical Trials job openings:
What are the most commonly searched types of Clinical Trials jobs? The most popular types of Clinical Trials jobs are:
What states have the most Weekend Clinical Trials jobs? States with the most job openings for Weekend Clinical Trials jobs include:
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
Under limited supervision, responsible for assisting with the administration, organization and implementation of trial operations, systems management, and training/education. Provides specialized and technical reviews of clinical trial research protocols, funding agreements and billing processes.
- 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.
What UT Health San Antonio employees say
Pay
Benefits
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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