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Clinical Research Coverage Analyst Jobs in Colorado

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Senior Clinical Research Associate

Denver, CO · On-site

$110K - $138K/yr

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

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All JobsClinical Research Coverage Analyst JobsClinical Research Coverage Analyst Jobs in Colorado

Clinical Research Coverage Analyst information

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$18

$41

$65

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

As of Aug 18, 2026, the average hourly pay for clinical research coverage analyst in Colorado is $41.85, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $48.03 per hour, depending on experience, location, and employer.

What is a clinical research coverage analyst?

A Clinical Research Coverage Analyst is responsible for reviewing clinical trial protocols, budgets, and billing plans to determine which services are billable to insurance and which should be covered by study sponsors. They ensure compliance with federal regulations, institutional policies, and Medicare coverage analysis (MCA) guidelines. Their role helps prevent billing errors, reduces financial risk, and supports proper funding allocation for clinical research studies. They collaborate with researchers, billing teams, and regulatory staff to streamline the financial and operational aspects of clinical trials.

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

Success as a Clinical Research Coverage Analyst requires strong knowledge of clinical research billing, healthcare regulations (such as Medicare Coverage Analysis), and a background in life sciences, healthcare administration, or a related field. Familiarity with clinical trial management systems (CTMS), electronic medical records (EMR), and compliance software, as well as relevant certifications like CCRC or ACRP, is highly valued. Attention to detail, critical thinking, and effective communication are vital soft skills for interpreting complex protocols and collaborating with cross-functional teams. These competencies help ensure regulatory compliance, accurate coverage analysis, and efficient trial operations.

What are some common challenges faced by clinical research coverage analysts, and how do they overcome them?

Clinical Research Coverage Analysts often encounter challenges such as interpreting complex study protocols, ensuring compliance with shifting regulations, and coordinating with various research and financial departments. To overcome these, analysts must stay current on regulatory updates, maintain clear communication with principal investigators and billing teams, and develop strong attention to detail. Many organizations provide ongoing training and foster a collaborative environment to support analysts in navigating these demands. By building expertise and leveraging team resources, analysts can accurately perform coverage analyses and ensure compliant trial billing.

What does a clinical research coverage analyst do?

A clinical research coverage analyst reviews and interprets insurance policies and coverage criteria related to clinical trials and medical procedures. They ensure that research activities comply with payer requirements, assist in billing processes, and help optimize reimbursement for clinical studies. Strong knowledge of healthcare regulations, coding, and documentation is essential for this role.

What are popular job titles related to Clinical Research Coverage Analyst jobs in Colorado?

For Clinical Research Coverage Analyst jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Clinical Research Coverage Analyst jobs in Colorado look for?

The top searched job categories for Clinical Research Coverage Analyst jobs in Colorado are:

Clinical Research Coverage Analyst jobs near you
Infographic showing various Clinical Research Coverage Analyst job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 1% Temporary, and 4% Contract. Highlights an 79% Physical, 1% Hybrid, and 20% Remote job distribution, with an average salary of $87,056 per year, or $41.9 per hour.

Clinical Research Coordinator

Quicksilver Scientific, Inc

Louisville, CO • On-site

$72K - $88K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Job description

Help advance the science behind innovative wellness solutions.
At Quicksilver Scientific, we're passionate about transforming health through cutting-edge nutritional science. Our research-backed products and advanced delivery technologies are changing the way practitioners and consumers approach wellness. As we continue to expand our scientific research initiatives, we're looking for a Clinical Research Coordinator who is organized, analytical, and excited to play a key role in bringing high-quality clinical research to life. If you thrive in a fast-paced environment, enjoy managing complex projects, and want your work to directly contribute to innovative health solutions, we'd love to hear from you.
What You'll Do
As our Clinical Research Coordinator, you'll oversee the planning, coordination, and execution of clinical research studies that support product innovation, scientific validation, and educational initiatives. You'll collaborate with cross-functional teams and external research partners to ensure studies are completed on time, within budget, and in compliance with regulatory standards.
Your Impact
Lead Clinical Research Studies
  • Coordinate clinical research studies from startup through closeout
  • Assist with study design, protocol development, and implementation
  • Partner with Clinical Research Organizations (CROs), investigators, laboratories, and academic institutions
  • Monitor study progress and proactively resolve issues that impact timelines or quality

Drive Project Success
  • Develop project timelines, budgets, and study documentation
  • Coordinate activities across multiple departments and external partners
  • Track milestones and communicate progress to stakeholders
  • Manage multiple research projects while balancing competing priorities

Support Study Participants
  • Coordinate participant recruitment, screening, enrollment, scheduling, and follow-up
  • Ensure informed consent is completed according to ethical and regulatory standards
  • Maintain participant confidentiality and accurate study records

Manage Clinical Data
  • Oversee data collection, validation, and organization
  • Ensure data accuracy, integrity, and compliance with Good Clinical Practice (GCP)
  • Perform quality reviews and assist with data analysis
  • Maintain organized, audit-ready study documentation

Ensure Regulatory Compliance
  • Maintain compliance with GCP, IRB requirements, and applicable regulations
  • Support protocol amendments, adverse event reporting, and regulatory submissions
  • Prepare for internal and external audits

Communicate Research Findings
  • Serve as the primary contact for assigned clinical studies
  • Prepare study updates, presentations, and research summaries
  • Present project progress to leadership and cross-functional teams

What You'll Bring
Required Qualifications
  • Bachelor's degree in Clinical Research, Biological Sciences, Healthcare, Public Health, Nursing, or a related scientific field
  • Minimum one year of clinical research or clinical study coordination experience
  • Experience managing projects involving multiple stakeholders
  • Strong Microsoft Office skills, especially Excel
  • AI acumen and the ability to leverage emerging technologies to improve efficiency
  • Excellent organizational, analytical, and communication skills

Preferred Qualifications
  • Two or more years of clinical research experience
  • CCRC or CCRP certification
  • Experience working with CROs, IRBs, or regulated clinical environments
  • Experience with Electronic Data Capture (EDC) or Clinical Trial Management Systems (CTMS)
  • Experience in the nutraceutical, supplement, pharmaceutical, or healthcare industry
  • Experience working in a growing, entrepreneurial company
  • Certified phlebotomist
  • Comfortable handling and processing human biologic specimens

Why You'll Love Working Here
At Quicksilver Scientific, science, innovation, and collaboration drive everything we do. We believe our employees are our greatest asset, and we invest in their success through meaningful work, outstanding benefits, and opportunities for growth.
Our Benefits Include
  • Competitive salary plus annual bonus opportunity
  • Comprehensive medical, dental, and vision insurance
  • Company-paid life insurance and disability coverage
  • 401(k) with company match
  • Generous Paid Time Off and paid company holidays
  • Generous employee product discounts
  • Summer Friday schedule (4½-day workweeks during the summer)
  • Collaborative, mission-driven culture focused on innovation and wellness

Work Schedule
Monday-Friday 8:30 AM-5:00 PM (Hours may vary based on business needs)
Why This Role Matters
Clinical research is at the heart of Quicksilver Scientific's commitment to delivering products backed by science. In this role, you'll help generate the evidence that supports product innovation, practitioner education, and consumer confidence. Your work will directly influence the future of wellness by ensuring every study is conducted with excellence, integrity, and scientific rigor. If you're passionate about clinical research and excited to make a meaningful impact in a growing, science-driven organization, we'd love to hear from you.
Join us in advancing the science of wellness.

Apply