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Full Time Remote Clinical Trial Jobs (NOW HIRING)

Fortrea

Clinical Trial Manager

Remote US or Canadian based. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

SummaryThe Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

Ionis

Clinical Trial Management Associate

Carlsbad, CA · On-site +1

$34.50 - $47.25/hr

We continue to invest time, money and energy into making our onsite, hybrid and remote work ... The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ...

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... This position is for remote work and may require domestic or international travel up to 25% (as ...

Icon plc

Senior Clinical Trial Manager

Blue Bell, PA · Remote

Senior Clinical Trial Manager (Oncology) - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

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Full Time Remote Clinical Trial information

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

As of Jul 26, 2026, the average hourly pay for full time remote clinical trial 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.

How to make $100,000 a year working from home?

A full-time remote clinical trial professional can earn $100,000 annually by gaining specialized certifications, such as in clinical research or project management, and accumulating experience in roles like clinical research associate or project manager. Building expertise in data management, regulatory compliance, and using industry tools can also increase earning potential, especially with a consistent full-time schedule and strong performance.

What is the difference between Full Time Remote Clinical Trial vs Full Time Remote Clinical Research Coordinator?

AspectFull Time Remote Clinical TrialFull Time Remote Clinical Research Coordinator
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar degrees; often holds certifications like CCRP or CRC
Work EnvironmentConducted remotely, managing trial data, documentation, and communication with sitesPrimarily remote; coordinates trial activities, site management, and patient interactions
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, CROs

While both roles involve clinical trial activities, the Full Time Remote Clinical Trial focuses on data management and trial oversight remotely, whereas the Clinical Research Coordinator handles site coordination and patient interactions, often requiring similar credentials and working in related environments.

How can I make $2000 a week working from home?

A full-time remote clinical trial role can offer competitive pay, potentially reaching $2000 per week depending on the trial phase, responsibilities, and experience. Earning this amount may require managing multiple trials, possessing relevant certifications, and working full-time hours in a structured environment. Building skills in clinical research, data management, and regulatory compliance can enhance earning potential.

Which clinical trials pay the most money?

Full time remote clinical trial roles that involve high levels of responsibility, such as clinical research managers or senior coordinators, tend to offer higher pay. Additionally, roles requiring specialized skills, certifications, or experience in areas like pharmacovigilance or regulatory affairs generally provide higher compensation in the clinical trial industry.
What cities are hiring for Full Time Remote Clinical Trial jobs? Cities with the most Full Time Remote Clinical Trial job openings:
What are the most commonly searched types of Remote Clinical Trial jobs? The most popular types of Remote Clinical Trial jobs are:
Full Time Remote Clinical Trial jobs near you
Clinical Trial Manager

Clinical Trial Manager

Fortrea

Remote

Full-time

Posted 17 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 72 rated research

Job description

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. Remote US or Canadian based.
Job Overview:
The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.
The role generally works under the direction of a (Senior) Clinical Trial Manager, however, may also work independently at a lower complexity study.
Summary of Responsibilities:
  • End-to-end oversight of start-up and clinical responsibilities-from site identification through to database lock-through proactive management of project scope, timelines, milestones, and budget.
  • Ensure start-up and clinical project plans address identified risks while adhering to professional standards, SOPs, client, and regulatory requirements.
  • Proactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems.
  • Responsible for financial aspects of clinical and start-up activities, including revenue forecasting, adherence to contracted scope, and oversight of scope modifications.
  • Ensure project team awareness and tracking of Key Project Indicators (KPI) for any client-specific start-up and clinical metrics.
  • Ensure and plans for start-up and clinical resources with accurate projections for the resourcing teams.
  • Develop and implement the site activation and recruitment strategy in collaboration with project teams.
  • Lead and oversee site identification and site selection.
  • Oversight of Informed Consent Form development and translations.
  • Oversight of essential document creation and collection, including insurance.
  • Oversight of the development, negotiation, and execution of Clinical Trial Agreements (CTA), including site budgets.
  • Lead the end-to-end process of regulatory/ethics committee submissions, approvals, and tracking.
  • Ensure clinical and ancillary supplies -including import/export logistics and supply destruction processes- are in place as applicable.
  • Manage operational aspects to support subject recruitment and retention, patient safety, vendor performance, and the monitoring visit strategy.
  • Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint protection.
  • Ensure inspection-readiness through quality oversight of TMF, monitoring reports, protocol deviations and issue management.
  • Oversight and approval of site payments, including payment reconciliation.
  • Foster effective communication and collaboration with clients and cross-functional project teams in a global and multicultural environment.
  • Ability to lead client-facing calls to communicate project status updates and demonstrate operational control of start-up and clinical deliverables.
  • Support new business with active participation in pre-award preparation as required.
  • Provide feedback on team members as needed to respective line managers.
  • All other duties as needed or assigned.

Qualifications (Minimum Required):
  • University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
  • Fluent in English, both written and verbal

Experience (Minimum Required):
  • Four or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.
  • Previous SSU and Clinical Trial Lead experience
  • Comprehensive knowledge of GCP, ICH, and regulatory guidelines.
  • Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).
  • Effective leadership in remote and global environment.
  • Strong communication, planning, and organizational abilities.
  • Proven team motivational skills.
  • Proficiency in balancing concurrent tasks within time-sensitive environments.
  • Financial awareness and use of tracking systems/tools.
  • Demonstrated independent problem-solving and risk management mindset.
  • Demonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.

In this role, employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training, without altering the fundamental nature or classification of the position.
Preferred Qualifications Include:
  • Master's or other advanced degree.
  • PMP certification or equivalent.

Physical Demands / Work Environment:
  • Remote-based work required with possible office presence depending on location.
  • Travel requirements: up to 20% (global - primarily domestic and international)

Pay Range: $140,000-148,000 USD annually
Learn more about our EEO & Accommodations request here.

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