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Full Time Remote Clinical Trials Jobs (NOW HIRING)

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview We are seeking an experienced Clinical Trials Manager (CTM) to oversee the clinical operational and ...

Natera

Senior Manager, Clinical Trials

$141K - $176K/yr

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to ... Remote USA $141,300-$176,600 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA ...

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 ...

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site +1

$157K - $203K/yr

Clinical Operations leads the global execution of Phase I-IV clinical trials across therapeutic ... Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ...

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Full Time Remote Clinical Trials information

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How much do full time remote clinical trials jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for full time remote 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 Full Time Remote Clinical Trials vs Full Time Remote Clinical Research Coordinators?

AspectFull Time Remote Clinical TrialsFull Time Remote Clinical Research Coordinators
CredentialsTypically requires a degree in life sciences, nursing, or related fields; certifications like CCRP are commonSimilar credentials, often with certifications like CCRP or CRC
Work EnvironmentConducts or oversees clinical trials remotely, often collaborating with sites and sponsorsCoordinates trial activities, manages data, and communicates with sites remotely
Industry UsageUsed by pharmaceutical companies, CROs, and research institutionsCommonly employed by research organizations and sponsors for trial management

Both roles involve remote work in clinical research, requiring similar credentials and industry usage. Full Time Remote Clinical Trials focus on overseeing or conducting entire trials, while Clinical Research Coordinators handle day-to-day trial coordination and data management. Understanding these differences helps job seekers find the right fit in the remote clinical research field.

Can you make a living doing full time remote clinical trials?

Full time remote clinical trial roles can provide a stable income, especially for experienced professionals such as clinical research coordinators or data managers. Salaries vary based on experience, location, and specific responsibilities, but many remote positions offer competitive pay and benefits, making it possible to make a living in this field with the right skills and certifications.
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Cities with the most Full Time 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 Full Time Remote Clinical Trials jobs?

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

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The top searched job categories for Full Time Remote Clinical Trials jobs are:

Full Time Remote Clinical Trials jobs near you
Infographic showing various Full Time Remote Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Manager- Remote

Chapel Hill, NC • Remote

Adecco
Recruiting and Staffing Services • 10K+ employees
Learn more about Adeccoexternal

$62 - $64.73/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

Clinical Trials Manager (CTM)

Location: Remote
Schedule: Full-Time | Eastern Time Zone Hours
Pay: $62.00–$64.73 per hour

Position Overview

We are seeking an experienced Clinical Trials Manager (CTM) to oversee the clinical operational and quality aspects of assigned clinical studies. This role is responsible for ensuring clinical deliverables are completed on time, within scope, and to quality standards, while supporting patient recruitment, study performance, and overall trial execution.

The ideal candidate will have strong clinical operations experience, excellent leadership and organizational skills, and a solid understanding of ICH/GCP, FDA regulations, clinical monitoring, and patient recruitment strategies.

Key Responsibilities

  • Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations.

  • Develop and maintain clinical tools, monitoring plans, guidelines, and study documentation.

  • Support development and maintenance of the Trial Master File (TMF) and ensure document quality and completeness.

  • Collaborate with Project Managers, clinical teams, data management, and other departments to meet study deliverables.

  • Lead clinical team meetings and ensure timelines, resources, communication, and quality objectives are maintained.

  • Monitor clinical timelines, metrics, site performance, and study progress.

  • Review monitoring reports, oversee CRF collection and query resolution, and implement recovery actions when needed.

  • Support patient recruitment strategies and work with study sites to address recruitment and retention challenges.

  • Communicate with study sites regarding protocol requirements, patient participation, CRFs, and study-related issues.

  • Coordinate study start-up activities and support timely ethics committee and regulatory submissions.

  • Ensure essential documents meet regulatory and quality requirements.

  • Support clinical resource planning, delegation of responsibilities, and identification of additional staffing needs.

  • Provide regular project status updates and contribute to client meetings and presentations.

  • Support forecasting, budgeting, and management of clinical project resources.

  • Ensure timely archiving of study documents and materials.

Qualifications

  • Bachelor's degree or equivalent relevant education.

  • 5+ years of relevant clinical research/clinical operations experience or comparable experience.

  • Strong understanding of ICH/GCP, FDA guidelines, and clinical trial requirements.

  • Experience with clinical monitoring practices and study operations.

  • Demonstrated experience with patient recruitment and retention strategies.

  • Strong leadership, mentoring, and team-building skills.

  • Excellent planning, organization, and prioritization abilities.

  • Strong problem-solving, judgment, and decision-making skills.

  • Ability to work effectively in a multicultural, matrixed, and changing environment.

  • Strong written and verbal communication skills.

  • Excellent attention to detail and ability to manage multiple priorities.

  • Working knowledge of Outlook, Excel, Word, and clinical research systems.

  • Understanding of budgeting, forecasting, resource allocation, and financial management preferred.

Work Arrangement

  • 100% Remote

  • Must be available to work Eastern Time Zone hours.

  • Full-time position.

Pay Rate: $62.00–$64.73/hour


Pay Details: $62.00 to $64.73 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.