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Part Time Clinical Research Coverage Analyst Jobs

On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare ...

On-site Schedule: Part-time (24 hours per week) Shape the Future of Medicine with IQVIA! Are you ... About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ...

Onsite Schedule: 24 Hours/Week (Parttime) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical ...

On-site Employment Type: Part-time - 24 Hours per Week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving health ...

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Part Time Clinical Research Coverage Analyst information

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$18

$39

$62

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

As of Jul 14, 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:
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 Assistant (Must Live in Los Angeles and Speak Spanish)

Angel City VA

Los Angeles, CA • On-site

Part-time

Re-posted 28 days ago


Job description

Title: Part time Clinical Research assistant
Job Summary:
The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc.
Education/Experience/Skills:
• High school graduate or equivalent. Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.

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