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Locum Clinical Trial Coverage Analyst Jobs (NOW HIRING)

ICON

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

As a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical ... analysis process at the study level and may perform reconciliation and/or tracking of sample ...

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of ... Frontier offers a competitive total rewards package which includes healthcare coverage, 401k and a ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Review and analyze clinical trial data to identify trends and potential issues. * Ensure tracking and review of protocol deviations and assess impact on study data * Develop relationships with ...

IQVIA

Clinical Trial Rater

Parsippany, NJ · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Los Angeles, CA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Houston, TX · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

IQVIA

Clinical Trial Rater

Boston, MA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... analytics, technology solutions, and clinical research services. We collaborate with top ...

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How much do locum clinical trial coverage analyst jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for locum clinical trial coverage 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 are the most commonly searched types of Clinical Trial Coverage Analyst jobs?

The most popular types of Clinical Trial Coverage Analyst jobs are:

Locum Clinical Trial Coverage Analyst jobs near you
Infographic showing various Locum Clinical Trial Coverage Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 10% Part Time, and 5% Contract. Highlights an 83% Physical, 1% Hybrid, and 16% 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

Re-posted yesterday

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