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Clinical Trial Analyst Jobs (NOW HIRING)

410 ICR United States USA

Clinical Trial Liaison

Blue Bell, PA

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

410 ICR United States USA

Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

IQVIA, Inc.

Clinical Trial Lead

Durham, NC · On-site

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... analysis and communication on a trial level as applicable. • Lead or contribute to corporate ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... Perform continuous review, risk identification, evaluation/ analysis and communication on a trial ...

PTC Therapeutics

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations ... Analytical thinker with excellent problem-solving skills and the ability to adapt to changing ...

Ptc Therapeutics, Inc.

Clinical Trial Associate I

Warren, NJ

$34.75 - $47.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations ... Analytical thinker with excellent problem-solving skills and the ability to adapt to changing ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... analysis timelines). * Assist with the review of central and third-party lab documents (e.g. Lab ...

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA · On-site

  • Medical

  • Retirement

  • PTO

Contribute to the development of site feasibility questionnaires and analysis of the feasibility results. * Manage day-to-day relationships with clinical trial vendors, including tracking vendor ...

Olema Oncology

Senior Clinical Trial Associate

Boston, MA · On-site

$110K - $115K/yr

About the Role >>> Senior Clinical Trial Associate As the Senior Clinical Trial Associate reporting ... Conducts oversight of sample collection, shipment, and analyses * Conducts reconciliation and ...

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA · On-site

$175K - $195K/yr

Vor Biopharma is seeking a Clinical Trial Manager/Sr. Clinical Trial Manager who will be ... Conduct project risk analysis and develops risk mitigation strategies for a variety of complex ...

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Clinical Trial Analyst information

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How much do clinical trial analyst jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for clinical trial analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

What does a clinical trial analyst do?

A Clinical Trial Analyst is responsible for managing and analyzing data collected during clinical trials to ensure accuracy and compliance with regulatory standards. They work closely with clinical research teams to monitor trial progress, identify trends, and help ensure that study protocols are being followed. Their work supports the evaluation of the safety and effectiveness of new drugs, treatments, or medical devices. Clinical Trial Analysts also assist with preparing reports and documentation for regulatory agencies and internal stakeholders.

What are the key skills and qualifications needed to thrive as a clinical trial analyst?

To thrive as a Clinical Trial Analyst, you need a background in life sciences or related fields, strong analytical skills, and experience with clinical research protocols. Familiarity with data management systems, statistical software (such as SAS or SPSS), and regulatory compliance tools (e.g., FDA or ICH guidelines) is typically required. Attention to detail, effective communication, and problem-solving abilities help you collaborate with cross-functional teams and ensure data integrity. These skills are crucial for accurately analyzing trial data, maintaining compliance, and supporting the successful execution of clinical studies.

What are some common challenges faced by clinical trial analysts when managing multiple studies simultaneously?

Clinical Trial Analysts often juggle data from several studies at once, which can present challenges like managing competing deadlines, ensuring data accuracy, and maintaining clear communication with cross-functional teams. Prioritizing tasks and staying organized are essential for meeting regulatory timelines and preventing errors. Additionally, adapting quickly to protocol changes or unexpected issues is a key part of the role, as is collaborating with data managers, statisticians, and clinical operations teams to keep studies on track.

What is the difference between Clinical Trial Analyst vs Clinical Research Coordinator?

AspectClinical Trial AnalystClinical Research Coordinator
Required CredentialsBachelor's degree in life sciences, biostatistics, or related field; some roles may require certification in clinical researchBachelor's degree in health sciences, nursing, or related field; often requires certification in clinical research coordination
Work EnvironmentData analysis, report preparation, and monitoring clinical trial dataManaging trial logistics, patient recruitment, and site coordination
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, Clinical Trial Analysts focus on data analysis and reporting, whereas Clinical Research Coordinators handle trial logistics and patient management. Both positions require similar educational backgrounds and certifications, but their daily tasks and work environments differ significantly.

More about Clinical Trial Analyst jobs

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Cities with the most Clinical Trial Analyst job openings:

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Clinical Trial Analyst jobs near you
Infographic showing various Clinical Trial Analyst job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Clinical Trial Liaison

410 ICR United States USA

Blue Bell, PA

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 28 days ago

Job description

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 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