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Remote Clinical Trial Jobs (NOW HIRING)

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... Maintaining a logical and organized approach to execution #LI-Remote #LI-NITINMAHAJAN IQVIA is a ...

New

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

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 ...

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

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison - Mid- Atlantic ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Allen Spolden

Clinical Trial Associate

Manhattan, NY · Remote

$55K - $65K/yr

This is a remote position. This role offers the opportunity to support the planning and execution ... Support the day-to-day coordination of clinical trials. * Maintain and organize Trial Master File ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... Maintaining a logical and organized approach to execution #LI-Remote #LI-NITINMAHAJAN IQVIA is a ...

New

Icon plc

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

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

Parexel

Global Clinical Trial Leader - FSP

Seeking Clinical Trial Leaders in the US with Oncology and/or Inflammation Experience The Clinical Trial Leader (CTL) is a key member of Clinical Delivery Team nominated to a specific trial within ...

Fortrea

Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience. Job Overview: The Clinical Trial Manager has ownership in the clinical delivery and operational ...

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How much do remote clinical trial jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for 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.

What is a remote clinical trial?

A Remote Clinical Trial job involves managing or supporting clinical research studies from a remote location rather than on-site at a hospital or research facility. Responsibilities may include data management, patient monitoring, regulatory compliance, and coordinating trial activities. These roles are often held by clinical research associates, coordinators, or data analysts who use digital tools to oversee the trial process. Remote roles help improve accessibility and efficiency while maintaining compliance with regulatory standards.

What are the key skills and qualifications needed to thrive in a remote clinical trial role?

To thrive in a Remote Clinical Trial position, you need a strong background in clinical research, regulatory compliance, and data management—often supported by a degree in life sciences or health-related fields. Familiarity with electronic data capture (EDC) systems, clinical trial management software (CTMS), and certifications like GCP (Good Clinical Practice) are highly beneficial. Exceptional organizational skills, attention to detail, and proactive communication are essential soft skills for remote collaboration and project management. These abilities ensure accurate trial execution, compliance with protocols, and seamless teamwork across distributed environments.

What are some common challenges faced in remote clinical trial roles, and how can they be managed?

One of the main challenges in remote clinical trial roles is maintaining effective communication and collaboration with research teams, participants, and stakeholders across various locations. This can be managed by utilizing secure collaboration tools, scheduling regular virtual check-ins, and following clear documentation practices. Remote professionals may also face difficulties in monitoring protocol compliance and data integrity without onsite presence, making strong organizational skills and familiarity with virtual monitoring tools essential. Being proactive and adaptable helps you address issues promptly and ensures study milestones are met. With the right support and resources, remote clinical trial professionals can seamlessly contribute to successful trial outcomes.

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Cities with the most Remote Clinical Trial job openings:

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Remote Clinical Trial jobs near you
Infographic showing various Remote Clinical Trial 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 $130,034 per year, or $62.5 per hour.

Clinical Trial Liaison

ICON

Blue Bell, PA • On-site, Remote

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 25 days ago

Job description

Clinical Trial Liaison
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What you will do:
Clinical Investigator Management
  • Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout
  • Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements
  • Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas
  • Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives
  • Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc
  • Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct

Clinical Trial Management
  • Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery
  • Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones
  • Drive inspection readiness as a continuous discipline across sites
  • Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality
  • Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization
  • Provide oversight and quality assurance for vendor monitoring, escalating risks proactively
  • Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations
  • Business Management and Engagement
  • Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials
  • Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner
  • Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity
  • Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution
  • Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel
  • Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer
  • Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships

You are:
  • Bachelor's degree or equivalent; strong preference for scientific, clinical, or health-related fields
  • Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites
  • Open to up to 60-80% travel during peak times (travel will vary)
  • Oncology experience required (Breast/Gyn experience preferred)
  • Location: Mid-Atlantic, Southeast Region

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$110,520.00-$138,150.00
Are you a current ICON Employee? Please click here to apply

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