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Freelance Remote Clinical Trials Jobs (NOW HIRING)

Moffitt

MGR CLINICAL TRIALS OFFICE

Chicago, IL · On-site +1

Summary This position will be on site/remote This will be for our Hematology/Myeloid team. Position ... the Clinical Trials Business Office and Research Finance to coordinate budget development and ...

Moffitt

MGR CLINICAL TRIALS OFFICE

Chicago, IL · On-site +1

Summary This position will be on site/remote This will be for our Lymphoma/Myeloma team. Position ... the Clinical Trials Business Office and Research Finance to coordinate budget development and ...

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Freelance Remote Clinical Trials information

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How much do freelance remote clinical trials jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for freelance remote clinical trials in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a freelance remote clinical trials specialist?

To thrive as a Freelance Remote Clinical Trials Specialist, you need a background in medical research, clinical trial protocols, and regulatory compliance, often supported by a degree in life sciences or related certification such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and trial management software is essential. Strong organizational skills, self-motivation, and effective communication set top performers apart, especially when collaborating remotely across teams. These competencies ensure accurate data collection, regulatory adherence, and successful trial outcomes in a flexible, virtual environment.

What is the difference between Freelance Remote Clinical Trials vs Clinical Research Coordinator?

AspectFreelance Remote Clinical TrialsClinical Research Coordinator
CredentialsVaries; often requires knowledge of clinical trials, certifications optionalTypically requires a bachelor's degree in health or related field, and certification
Work EnvironmentRemote, flexible, project-basedOn-site or hybrid at research sites or hospitals
Employer & Industry UsageFreelance platforms, biotech, pharma companiesHospitals, research institutions, pharmaceutical companies
Search & Comparison IntentHigh overlap in trial management, patient coordination, data collectionFocus on site management, patient interaction, regulatory compliance

Freelance Remote Clinical Trials professionals typically work independently on trial projects, often remotely, with flexible hours. Clinical Research Coordinators usually work on-site at research facilities, managing daily trial activities. Both roles involve clinical trial processes but differ mainly in work setting and employment structure.

What is a freelance remote clinical trials specialist?

Freelance remote clinical trials involve independent professionals who work remotely to support or manage various aspects of clinical research studies. These roles can include data management, regulatory documentation, patient recruitment, monitoring, and more, all performed outside of a traditional office or onsite setting. Freelancers in this field often collaborate with pharmaceutical companies, contract research organizations (CROs), and academic institutions, using digital tools to conduct and oversee trial activities from any location. This flexible arrangement allows for a wider range of expertise and can help speed up the clinical trial process. Remote clinical trials are increasingly popular due to advances in technology and the need for decentralized research.

What are some common challenges faced by freelance remote clinical trials specialists, and how can they be addressed?

Freelance remote professionals in clinical trials often encounter challenges such as coordinating across multiple time zones, maintaining clear communication with dispersed teams, and ensuring compliance with regulatory standards without in-person supervision. To address these issues, it's important to set up reliable digital communication channels, proactively schedule regular check-ins, and stay updated on industry regulations. Utilizing project management and collaboration tools can also streamline workflows and help maintain data integrity throughout the trial process.
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Cities with the most Freelance Remote Clinical Trials job openings:

What are the most commonly searched types of Remote Clinical Trials jobs?

The most popular types of Remote Clinical Trials jobs are:

What states have the most Freelance Remote Clinical Trials jobs?

States with the most job openings for Freelance Remote Clinical Trials jobs include:

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Freelance Remote Clinical Trials jobs near you
Infographic showing various Freelance Remote Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

MGR CLINICAL TRIALS OFFICE

Moffitt

Chicago, IL • On-site, Remote

Full-time

Re-posted 17 days ago

Job description

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times' Top Workplaces.

Summary

This position will be on site/remote This will be for our Hematology/Myeloid team. Position Highlights: Responsible for the direct supervision of clinical research staff Leads the daily clinical research operations for one or more key areas Responsible for monitoring workloads and determining appropriate staffinglevels for the clinical research staff (nurses, coordinators, and data specialists) Takes the lead and/or participates in development and execution oftraining/mentoring programs, quality improvement processes and other projects, including the development of SOP's Works in collaboration with the Clinical Trials Business Office and Research Finance to coordinate budget development and research patient and sponsor billing Responsible for budgeting and financial management of one or more cost centers Responsibilities: Staff supervision and mentoring, monitor staff conduct, perform staff interviews, recommend hire/terminations, and perform annual staff evaluations Allocates staff based on patient acuity, staffing standards and expertise of personnel Fiscal oversight-develop annual budget for the Clinical Trials Office cost center, review individual protocol budgets to assure adequate data management reimbursement; responsible for revenue creation, cost management and purchasing Actively participate in operational review of new protocols and amendments for feasibility of conduct Assist with development, revision and continuous evaluation of clinical research department standards and policies; participate in and/or lead process improvement working groups and staff mentoring education activities Credentials and Qualifications: Bachelor's degree (Master's preferred) Five (5) years of experience in executing multidisciplinary clinical research protocols (preferably in oncology) Two (2) years of staff supervisory/management experience Clinical Research Certification (e.g. SOCRA, ACRP) preferred

Salary Range

Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.


We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.

Moffitt Career Site

If you have the vision, passion, and dedication to contribute to our mission,then we have a place for you!

1. Equal Employment Opportunity

Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.

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Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email atHRReceptionists@moffitt.org. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

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