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Part Time Clinical Research Coverage Analyst Jobs

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Part Time Clinical Research Coverage Analyst information

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$62

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

As of May 29, 2026, the average hourly pay for part time clinical research 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 key skills and qualifications needed to thrive as a Part Time Clinical Research Coverage Analyst, and why are they important?

To thrive as a Part Time Clinical Research Coverage Analyst, you need a strong understanding of clinical research protocols, medical billing, and healthcare regulations, often supported by a bachelor’s degree in a health-related field. Familiarity with clinical trial management systems (CTMS), Medicare coverage analysis tools, and regulatory compliance software is typically required. Attention to detail, analytical skills, and effective communication are crucial soft skills for interpreting complex documents and collaborating with research teams. These competencies ensure accurate financial analysis, regulatory compliance, and efficient support of clinical research operations.

What are the primary challenges a Part Time Clinical Research Coverage Analyst may face when balancing multiple studies with limited hours?

As a Part Time Clinical Research Coverage Analyst, you may find it challenging to manage the workload of reviewing and analyzing coverage for several clinical trials within a restricted schedule. Prioritizing tasks and maintaining clear communication with coordinators and principal investigators are essential to ensure all studies remain compliant and deadlines are met. Effective time management and familiarity with relevant regulations help in balancing accuracy with efficiency, while collaboration with billing and compliance teams supports the resolution of complex coverage issues.

What does a Part Time Clinical Research Coverage Analyst do?

A Part Time Clinical Research Coverage Analyst is responsible for reviewing clinical research studies to determine which costs can be billed to insurance and which must be covered by research funds. They analyze study protocols, ensure compliance with federal and institutional regulations, and work closely with clinical and billing teams. This role is crucial in making sure that research billing is handled accurately, helping prevent billing errors and ensuring that clinical trials are conducted ethically and within legal guidelines.
More about Part Time Clinical Research Coverage Analyst jobs
What cities are hiring for Part Time Clinical Research Coverage Analyst jobs? Cities with the most Part Time Clinical Research Coverage Analyst job openings:
What are the most commonly searched types of Clinical Research Coverage Analyst jobs? The most popular types of Clinical Research Coverage Analyst jobs are:
What states have the most Part Time Clinical Research Coverage Analyst jobs? States with the most job openings for Part Time Clinical Research Coverage Analyst jobs include:
Infographic showing various Part Time Clinical Research Coverage Analyst job openings in the United States as of May 2026, with employment types broken down into 3% As Needed, 91% Full Time, 3% Part Time, and 3% Temporary. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.
Clinical Research Coordinator I (Temporary/Part-Time)

Clinical Research Coordinator I (Temporary/Part-Time)

Inbios International Inc

Seattle, WA • On-site

$26.44 - $31.25/hr

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago


Job description

Job Type
Part-time, Temporary
Description
Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.
About Us
InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.
Location: Seattle, WA
Type: Part-Time (30 hours per week), Temporary (6-months) Hybrid
This is a project-based position funded by a federal contract. If selected for the position, you will be hired as a temporary, part-time employee and the term of employment is dependent upon ongoing funding.
Position Wage Range: $26.44 - $31.25/per hour
What You'll Do
We're looking for a temporary, part-time Clinical Research Coordinator to support clinical studies and international product registration. The successful candidate must have a BS in a scientific discipline, have familiarity with Good Clinical Practice (GCP) and have excellent attention to details as well as good communication skills but written and verbal.
Key Responsibilities
Clinical Site Monitoring
  • Under the direction of the Project Manager assist in the maintenance of regulatory binders and Institutional Review Board (IRB) submissions.
  • Monitor clinical study to ensure that all participant records entered into the electronic data capture system are accurate and follow the clinical protocol and source documents.
  • Participate in Site Initiation training (SIV), monitor study compliance, and assist with study closeout.
  • Ensure that participants enrolled in the study meet the inclusion/exclusion criteria.
  • Monitor and report protocol deviations and adverse events in a timely manner.
  • Participate in study site close-out.
Product Registrations (International)
  • Identify regulatory requirements for product registrations worldwide.
  • Review analytical and clinical data against country regulatory requirements and identify gaps that need to be filled to obtain product registration.
  • Assist in the preparation of technical files in compliance with IVDR.
What We're Looking For
Required
  • Bachelor's degree in a scientific discipline.
  • Strong attention to detail, excellent written and verbal communication, and proficiency with technology (e.g., MS Office, Electronic Database Systems).
  • Knowledge of ICH GCP guidelines. GCP certification.
  • Entry-level knowledge of IVDR requirements for medical devices.
Preferred
  • 1- to 3-year experience in project management.
  • Certified Clinical Research Associate credential.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • Prorated paid holidays and sick time as applicable to term of employment and work schedule in accordance with policies stated in the Company's employee handbook.
  • Supportive, mission-driven culture

Apply Today
Be part of a team that's advancing science and improving lives.