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Weekend Clinical Trials Jobs (NOW HIRING)

Kelly Services

Clinical Trials Nurse

Newport News, VA · On-site

Work among top multidisciplinary teams at the intersection of research and military healthcare Ready to make your mark at the cutting-edge of military and federal clinical trials? Submit your resume ...

ImmunityBio

Clinical Trials Manager

Culver City, CA

$145K/yr

Essential Functions * Assist in the development and management of company-sponsored clinical trials * Assist in reviewing completed assignments by members of the clinical development group * Assist ...

ImmunityBio, Inc.

Clinical Trials Manager

$145K/yr

Essential Functions * Assist in the development and management of company-sponsored clinical trials * Assist in reviewing completed assignments by members of the clinical development group * Assist ...

CG Oncology, Inc.

Senior Clinical Trials Scientist

$150K - $170K/yr

About the role The Senior Clinical Trials Scientist (Sr CTS) provides scientific leadership and mentorship across Clinical Development and Operations teams but does not include formal line management ...

Access Community Clinical Trials

Be Seen First

Clinical Research Nurse

Abilene, TX · On-site

Abilene, Texas Employment Type: Part-Time Access Community Clinical Trials (ACCT) is a growing ... weekends based on protocol-specific infusion schedules and subject needs. * Moderate to high ...

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Weekend Clinical Trials information

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How much do weekend clinical trials jobs pay per hour?

As of Jun 10, 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?

AspectWeekend Clinical TrialsPart-Time Clinical Research Coordinator
CredentialsTypically requires clinical trial experience, basic medical knowledgeRequires certification in clinical research or related field, experience preferred
Work EnvironmentConducted at research sites, hospitals, or clinics during weekendsOffice-based, overseeing trial activities, often flexible hours
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, clinical trial sites
Search & Comparison IntentUnderstanding weekend trial roles, flexible clinical trial workPart-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:
Weekend Clinical Trials jobs near you
SPVR CLINICAL TRIALS OFFICE

SPVR CLINICAL TRIALS OFFICE

H. Lee Moffitt Cancer Center

Tampa, FL • On-site

Full-time

Posted 29 days ago

Moffitt Cancer Center rating

8.1

Company rating: 8.1 out of 10

Based on 92 frontline employees who took The Breakroom Quiz

70th of 870 rated healthcare providers

Job description

Job Summary

 Position Highlights:

  • Provides basic day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible CTO manager and in collaboration with faculty and investigators.  
  • Works effectively across the organization and externally with sponsor organizations to ensure effective and efficient conduct of clinical research.
  • Supports the recruiting, training, development, and performance management of assigned staff.
  • Operationally focuses on study start up, trial coordination, and quality assurance needs, providing problem-solving and troubleshooting expertise.
  • Will be expected to identify process improvement opportunities, collaborate with their team to develop creative solutions, lead/delegate implementation, and track success through defined metrics.

Responsibilities:

  • Provide daily supervision of research staff including scheduling to meet program business needs and orientation and training.
  • Supervise the staff responsibilities for the clinical aspects of study start up.
  • Serve as resource to investigators writing investigator-initiated trials.
  • Perform quality assurance procedures to check work of assigned staff for accuracy and completeness.
  • Work with the CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.   

Credentials and Qualifications:

  • Bachelor's degree.
    • (Science or Health care related field preferred; Masters preferred)
  • SoCRA or ACRP (or equivalent) certification.
  • Four (4) years experience in clinical trials (patient facing coordination, data management, regulatory, or other research coordination).
  • Oncology trials knowledge, OnCore CTMS experience preferred. 
  • Supervisory, or team lead experience preferred

What Moffitt Cancer Center employees say

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