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Clinical Trial Coverage Analyst Jobs (NOW HIRING)

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Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

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Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

Kailera Therapeutics, Inc.

Clinical Trial Manager

Waltham, MA · On-site

$127K - $155K/yr

  • Medical

  • Life

  • Retirement

Must have strong clinical study management, communication (oral and written), and analytical skills ... We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

New

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 ...

New

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 ...

New

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 ...

New

IQVIA

Clinical Trial Rater

Durham, NC · 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 ...

New

IQVIA

Clinical Trial Rater

New York, NY · 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 ...

New

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 · On-site

$120K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

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All JobsClinical Trial Coverage Analyst Jobs

Clinical Trial Coverage Analyst information

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

As of Aug 19, 2026, the average hourly pay for 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 is a clinical trial coverage analyst?

A Clinical Trial Coverage Analyst is responsible for reviewing clinical trial protocols and budgets to determine the extent of insurance coverage and compliance with federal regulations. They analyze whether trial-related procedures are billable to insurance or should be covered by the study sponsor. This role involves collaborating with research teams, compliance officers, and billing departments to ensure accurate financial planning and regulatory adherence. Strong knowledge of Medicare coverage analysis, FDA regulations, and healthcare billing practices is typically required.

What are the typical daily responsibilities of a clinical trial coverage analyst?

Clinical Trial Coverage Analysts are responsible for reviewing clinical trial protocols to determine which procedures and services are billable to insurance and which are covered by study sponsors. They regularly interact with research coordinators, billing teams, and compliance officers to clarify coverage determinations and resolve any discrepancies. Analysts also document findings, maintain accurate records, and stay up-to-date with changes in insurance regulations. The role is collaborative and detail-oriented, often requiring coordination across multiple departments to ensure clinical trial billing is accurate and compliant.

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

A Clinical Trial Coverage Analyst needs strong knowledge of clinical research protocols, health insurance guidelines, and medical terminology, often backed by a degree in health sciences or related fields. Familiarity with coverage analysis software, clinical trial management systems (CTMS), and compliance standards such as CMS or Medicare is essential. Attention to detail, analytical thinking, and effective communication are standout soft skills in this position. These competencies are vital for accurately determining coverage, ensuring regulatory compliance, and facilitating smooth collaboration across clinical and administrative teams.

What does a clinical trial coverage analyst do?

A clinical trial coverage analyst reviews and determines insurance coverage and reimbursement policies for clinical trials. They analyze healthcare plans, coordinate with providers, and ensure compliance with regulations to facilitate patient access and proper billing for trial-related services.
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Clinical Trial Coverage Analyst jobs near you
Infographic showing various Clinical Trial Coverage Analyst job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Clinical Trial Manager

Kailera Therapeutics, Inc.

Waltham, MA

Full-time

Posted 15 days ago

Job description

What You'll Do:

The Clinical Trial Manager will provide project support to team members by leading and/or participating in the daily management of clinical trial activities. Successful candidate will be working closely with and will be responsible for oversight of study activities through our CROs and service providers, including study start-up, conduct, and completion.
This position provides an opportunity to join a rapidly growing Clinical Operations organization and contribute substantially to the building of the department and the successful implementation of trials. 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Perform as the lead interface with the CRO regarding status of project activities and deliverables (including but not limited to site identification and selection, pre-study activities, enrollment, management/conduct, database lock, post-study activities)
  • Collaborate with the cross-functional clinical trial team to review and prepare various clinical study documents including but not limited to study protocol, model informed consent forms, and study plans
  • Lead day-to-day management of external vendors, as needed, to support the trial design and implementation
  • Review and approve internal and external vendor study plans and processes, as applicable
  • Review monitoring reports and interact with CRO to ensure the quality of monitoring and site management
  • Work with cross-functional team to ensure data query management and data retrieval is taking place in a timely manner
  • Review deviation listings and site audit reports and work with team to resolve site issues (e.g., staff retraining, additional resources)
  • Maintain and ensure the quality and completeness of study master files in compliance with GCP
  • Lead Clinical Study Team meetings internally, and/or with CRO and service providers

Required Qualifications:

  • Work experience to include a minimum of 6 years clinical trial experience with a solid understanding of functional area responsibilities associated with the clinical development process
  • Good working knowledge of ICH-GCP guidelines and regulatory requirements for clinical trial management
  • Must have strong clinical study management, communication (oral and written), and analytical skills
  • Excellent interpersonal skills, with a demonstrated ability to work in a team environment as well as independently
  • Additional attributes include an ability to multi-task, be flexible, and to thrive in a fast-paced environment
  • Demonstrated ability to effectively manage external vendors & CROs
  • Advanced proficiency in Microsoft Office and Microsoft Project or other Project Management software
  • Demonstrated strong written and verbal communication skills
  • Must be able to travel 

 

Education:

  • BA/BS; Life Science degree a plus

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