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Weekend Clinical Trials Jobs (NOW HIRING)

Stamford Health

Clinical Trials Manager-B

Stamford, CT · On-site

The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary ...

Stamford Health

Clinical Trials Manager-B

Stamford, CT · On-site

The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary ...

Gilead

Clinical Trials Manager

Foster City, CA · On-site

Clinical Operations plays a key role in ensuring allGilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high ...

Honorhealth

Manager - Clinical Trials

Scottsdale, AZ · On-site

Develops and implements departmental processes for the conduct of clinical trials. Tracks productivity within the clinical trial portfolio assigned. * Evaluates new protocols for operational ...

SAON LLC

Clinical Trials Manager

Shreveport, LA · On-site

Clinical Trials Manager Lead the team that runs our clinical research Location: Shreveport, LA (standard medical office; some local travel) Type: Full-time · Exempt · Reports to Principal/President ...

Houston Methodist

The Manager Clinical Trials position monitors progress and performance of all projects to include quality of services, timelines, financial viability, compliance with federal, state and/or other ...

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Weekend Clinical Trials information

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$96

How much do weekend clinical trials jobs pay per hour?

As of Sep 7, 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

Clinical Trials Manager-B

Stamford Health

Stamford, CT • On-site

Full-time

Medical, Retirement, PTO

Re-posted 26 days ago

Stamford Health rating

8.0

Company rating: 8.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

Job description


As a Certified Great Place to Work organization, Stamford Health understands what it takes to attract talent to improve our workforce and support our mission, to that end we offer:
• Competitive salary
• Comprehensive, low-cost health insurance plans (including GLP-1 coverage options) available day one
• Wellness programs
• Paid Time Off accruals
• Tax deferred annuity and (403b) pension plan
• Tuition reimbursement
• Free on-site parking and train station shuttle
• Childcare partnership with Children's Learning Center
Regular, Full Time Schedule (Monday-Friday, 37.5 Hours per week)
Responsibilities:
Under the direction of the Director of the Office of Research, the manager oversees
all aspects of the department as they relate to management of Oncology and non-Oncology Clinical Trials. The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary for the successful operation of clinical trials
• Seeks trial opportunities and/or receives, reviews and presents protocols for consideration by physicians. Reviews CDA and manages CDA process.
• Reviews contract, consent, budget, amendments, and other modifications to documentation for appropriateness.
• Acts as liaison between SH legal, clinical trials program and CRO/Sponsor to insure consistency of documents and compliance with department/institution's operating procedures.
• Negotiates budgets and affiliated scope of work. Also negotiates incidentals not covered under contract as necessary.
• Establishes study milestones within each protocol for collection purposes.
• Works closely with department's billing supervisor and department administrator to insure that research billing meets government and institutional guidelines, is billed timely and correctly.
• Trains staff to correctly report billing activity and monitors compliance with rules.
• Interfaces with billing department to prevent duplicate or missed billing.
• Maintains accurate and detailed accounting of inflow and outflow of funds through invoicing, client bill and income due from contractual agreements. Provides reporting as requested.
• Receive payments, identify appropriate disbursement of funds and work with Patient Access Supervisor to insure client bills are offset by funds received.
• Establish client bill parameters with other departments and properly instruct departments on billing of their services. Also give clear instruction to outside providers billing for services related to research.
• Monitor compliance of both service provider types.
• Analyzes and presents financial status.
Qualifications:
• Bachelor's degree required (Masters Preferred)
• Five years of prior relevant experience in an equivalent healthcare setting involving clinical trials.
• Exceptional computer literacy in a PC environment is required with strong organizational, interpersonal and communication skills.

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