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Part Time Clinical Research Coverage Analyst Jobs

University of Pennsylvania

$22.36 - $22.75/hr

The Center for Weight and Eating Disorders at the University of Pennsylvania Perelman School of Medicine seeks a part-time Clinical Research Coordinator (CRC). The candidate will help coordinate an ...

University of Pennsylvania

$22.36 - $22.75/hr

The Center for Weight and Eating Disorders at the University of Pennsylvania Perelman School of Medicine seeks a part-time Clinical Research Coordinator (CRC). The candidate will help coordinate an ...

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

As of Jul 13, 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 is the most entry level job in clinical research?

The most entry-level role in clinical research is often a Clinical Research Assistant or Coordinator, responsible for supporting study activities, data collection, and regulatory documentation. These positions typically require minimal experience, sometimes just a relevant degree or certification, and provide a pathway to more advanced roles in the field.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Clinical Research Director or Vice President of Clinical Operations tend to be the highest paying, often earning six-figure salaries. These positions require extensive experience, leadership skills, and often advanced certifications or degrees, and they oversee multiple projects or departments within pharmaceutical or biotech companies.

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.

Is CRC an entry level position?

A Part Time Clinical Research Coverage Analyst (CRC) is typically an entry-level to mid-level role, often suitable for individuals with some healthcare or research experience. The position may require knowledge of clinical trial processes, data management, and regulatory compliance, but it generally does not require extensive prior experience. Opportunities for training and certification, such as GCP or clinical research courses, can help candidates qualify for this role.

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 clinical research coverage analyst do?

A clinical research coverage analyst reviews and determines the appropriate billing and reimbursement policies for clinical trial procedures and services. They ensure compliance with healthcare regulations, analyze coverage policies, and collaborate with research teams and payers to facilitate accurate billing and documentation.

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 job categories do people searching Part Time Clinical Research Coverage Analyst jobs look for? The top searched job categories for Part Time Clinical Research Coverage Analyst jobs are:
Part Time Clinical Research Coverage Analyst jobs near you
Infographic showing various Part Time Clinical Research Coverage Analyst job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 86% Full Time, 6% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Clinical Research Accounts Billing Specialist

Salma Mazhar MD PA

Mesquite, TX • On-site

Part-time

Posted 7 days ago

New

Job description

Summary:
The Clinical Research Accounts Billing Specialist is responsible for managing the financial and billing activities related to clinical trials. This role ensures accurate invoicing, payment tracking, and compliance with study budgets, contracts, and sponsor requirements. The specialist works closely with clinical operations, sponsors, and finance teams to ensure timely and accurate revenue cycle management. THIS IS A PART TIME OPPORTUNITY.
Key Responsibilities:
  • Prepare, review, and submit invoices to sponsors and CROs based on clinical trial agreements and milestones
  • Reconcile study budgets with completed patient visits, procedures, and data entries (e.g., EDC systems)
  • Track accounts receivable and follow up on outstanding payments
  • Resolve billing discrepancies, denials, and payment variances
  • Maintain accurate financial records for each clinical study
  • Collaborate with study coordinators and project managers to verify subject visits and billable events
  • Ensure compliance with contracts, protocols, and regulatory requirements
  • Assist in budget development and coverage analysis when needed
  • Generate financial reports for management (aging reports, revenue tracking, etc.)
  • Support audits by providing required billing documentation

Required Qualifications:
  • Associate's or Bachelor's degree in Accounting, Finance, Healthcare Administration, or related field
  • 2+ years of experience in medical billing, clinical research billing, or healthcare finance
  • Strong understanding of clinical trial billing processes and sponsor invoicing
  • Experience with CRIO or other CTMS preferred
  • Proficiency in Microsoft Excel and accounting software
  • High attention to detail and strong organizational skills

Preferred Qualifications:
  • Experience working in a clinical research site, CRO, or sponsor environment
  • Knowledge of clinical trial agreements, budgets, and coverage analysis
  • Familiarity with Medicare billing rules related to clinical trials
  • Certification in clinical research (e.g., ACRP, SOCRA) is a plus

Key Skills:
  • Analytical and problem-solving skills
  • Strong communication and follow-up abilities
  • Time management and multitasking
  • Financial reconciliation and reporting
  • Knowledge of regulatory compliance in clinical research

Work Environment:
  • OFFICE BASED. Remote is not available.
  • May require coordination with multiple departments and external sponsors

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