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Senior Clinical Research Coverage Analyst Jobs (NOW HIRING)

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

What You'll Do As a senior clinical research professional, you will lead and support complex ... Participate in an established on-call research coverage rotation supporting critical care research ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

What You'll Do As a senior clinical research professional, you will lead and support complex ... Participate in an established on-call research coverage rotation supporting critical care research ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

By combining clinical research expertise with operational and business excellence, we help ... Conduct Medicare Coverage Analyses (MCA) for a mixture of oncology and non-oncology clinical trial ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... Manage and resolve data queries, analyze error trends, and provide targeted retraining to prevent ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Icon plc

Senior Clinical Research Associate

Chicago, IL · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

Icon plc

Senior Clinical Research Associate

Denver, CO · Hybrid

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare ... Life assurance and disability coverage * Employee assistance programmes and wellbeing resources

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Senior Clinical Research Coverage Analyst information

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$51K

$111.4K

$117.5K

How much do senior clinical research coverage analyst jobs pay per year?

As of Aug 14, 2026, the average yearly pay for senior clinical research coverage analyst in the United States is $111,445.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is the difference between Senior Clinical Research Coverage Analyst vs Clinical Research Coverage Analyst?

AspectSenior Clinical Research Coverage AnalystClinical Research Coverage Analyst
Required CredentialsBachelor's degree, experience in clinical research, knowledge of coverage analysisBachelor's degree, entry-level experience, understanding of clinical research processes
Work EnvironmentHealthcare organizations, research institutions, pharmaceutical companiesResearch sites, healthcare providers, insurance companies
Employer & Industry UsageUsed in clinical trial planning, reimbursement, and coverage determinationUsed in clinical trial support, coverage analysis, and documentation

The main difference between a Senior Clinical Research Coverage Analyst and a Clinical Research Coverage Analyst lies in experience level and responsibilities. The senior role typically involves more complex coverage analysis, mentorship, and strategic planning, while the entry-level analyst focuses on supporting coverage tasks. Both roles are essential in clinical research and healthcare settings, with the senior position requiring more expertise and industry knowledge.

What are some common challenges faced by senior clinical research coverage analysts and how can they be addressed?

Senior Clinical Research Coverage Analysts often encounter challenges such as navigating complex regulatory requirements, interpreting evolving billing guidelines, and ensuring accurate coverage analysis for clinical trials. Balancing the needs of study teams, finance, and compliance departments requires strong communication skills and meticulous attention to detail. Staying current with regulations and fostering collaborative relationships with both clinical and administrative staff can help address these challenges and ensure high-quality, compliant coverage analyses.

What does a senior clinical research coverage analyst do?

A Senior Clinical Research Coverage Analyst is responsible for reviewing clinical trial protocols to determine which costs are billable to insurance and which should be covered by the study sponsor. They analyze study documents, apply federal and institutional regulations, and work closely with research teams to ensure compliance. This role often involves preparing coverage analyses, educating staff on billing compliance, and serving as a resource for complex research billing questions.

What are the key skills and qualifications needed to thrive as a senior clinical research coverage analyst, and why are they important?

To excel as a Senior Clinical Research Coverage Analyst, you need a detailed understanding of clinical research protocols, medical billing, and regulatory compliance, typically supported by a bachelor's degree in a health-related field and experience in clinical research finance. Familiarity with Medicare Coverage Analysis (MCA) tools, electronic medical records (EMRs), and research management systems is essential. Strong analytical thinking, attention to detail, and effective communication are critical soft skills for interpreting complex documents and collaborating with multidisciplinary teams. These skills ensure accurate coverage determinations, regulatory adherence, and optimized financial operations for clinical trials.
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Senior Clinical Research Coverage Analyst jobs near you
Infographic showing various Senior Clinical Research Coverage Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, and 5% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $111,445 per year, or $53.6 per hour.

Senior Clinical Research Coordinator

Tekton Research Inc

Austin, TX • On-site

$24 - $32/hr

Full-time

Posted yesterday

New

Job description

Senior Clinical Research Coordinator - Austin, Texas

Full-Time/Non-Exempt/On-Site

Position Summary

The Senior Clinical Research Coordinator (Senior CRC) is an experienced clinical research professional responsible for managing multiple clinical trials from study start-up through close-out. This role ensures protocol compliance, participant safety, data integrity, regulatory compliance, and successful study execution.

The Senior CRC serves as a key liaison between investigators, sponsors, monitors, participants, and research staff while providing guidance and mentorship to junior coordinators. The ideal candidate is highly organized, proactive, detail-oriented, and able to effectively manage multiple priorities.

Key Responsibilities
  • Independently coordinate and manage multiple clinical trials from start-up through close-out.
  • Serve as a primary site contact for investigators, sponsors, monitors, vendors, and study teams.
  • Recruit, screen, consent, enroll, and retain study participants according to protocol requirements.
  • Conduct study visits and perform pediatric and adult phlebotomy and specimen processing as required.
  • Monitor participant safety and appropriately document and report adverse events and protocol deviations.
  • Maintain accurate source documentation, regulatory files, and essential study records in compliance with GCP, FDA regulations, and ICH guidelines.
  • Prepare and submit IRB and regulatory documents, including amendments and continuing reviews.
  • Maintain accurate study data in EDC and CTMS systems and resolve data queries within required timelines.
  • Prepare for and support monitoring visits, sponsor audits, and regulatory inspections.
  • Identify and resolve study issues proactively to maintain timelines, quality, and compliance.
  • Mentor and provide guidance to Clinical Research Coordinators and other research staff.
  • Contribute to process improvement and overall site quality and performance.
Required Qualifications
  • High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, Clinical Research, or related field preferred.
  • 3-5+ years of clinical research experience, with demonstrated ability to independently coordinate clinical trials.
  • Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical research processes.
  • Experience managing multiple clinical trials and competing priorities.
  • Experience with pediatric and adult phlebotomy and specimen processing.
  • Experience maintaining regulatory documentation and source records.
  • Proficiency with EDC systems, CTMS, and Microsoft Office.
  • Strong organizational, problem-solving, and communication skills.
  • Ability to work independently, exercise sound judgment, and collaborate effectively with multidisciplinary teams.
  • Commitment to participant safety, data integrity, and research quality.
Preferred Qualifications
  • Current ACRP or CCRC, or equivalent certification.
  • Bachelor's or advanced degree in a healthcare, public health, or clinical research field.
  • Experience with industry-sponsored and/or multi-center clinical trials.
  • Experience mentoring junior research staff.
  • Experience supporting sponsor audits, regulatory inspections, or complex monitoring activities.
  • Experience with participant recruitment and retention strategies.
Why Join Tekton Research?

At Tekton Research, you'll join a team dedicated to excellence, innovation, and improving lives through clinical research. We value professional development, collaboration, accountability, and meaningful contributions.

If you're an experienced clinical research professional ready to take on greater responsibility and help lead high-quality clinical trial execution, we encourage you to apply and become part of the Tekton Research team.