ZipRecruiter

Log In

2

Part Time Clinical Research Coverage Analyst Jobs

The Pennsylvania State University

$23.75 - $31.75/hr

Kristina Petersen's labin the Department of Nutritional Sciences is seekinga part-time Clinical Research Coordinator to support externally funded clinical trials investigating dietary interventions ...

Eisenhower

Clinical Research Coordinator

Rancho Mirage, CA · On-site

$24.75 - $32.75/hr

... budgets, coverage analysis, tracking of invoiceable term items and research billing. 10. Performs clinical site activities (regulatory issues, patient accrual, patient scheduling and care ...

next page

Showing results 1-20

All Jobspart time JobsPart Time Clinical Research Coverage Analyst Jobs

Part Time Clinical Research Coverage Analyst information

See salary details

$18

$39

$62

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

As of Aug 21, 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 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.

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 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.
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 August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 10% Part Time, and 5% Contract. Highlights an 79% Physical, 1% Hybrid, and 20% Remote job distribution, with an average salary of $82,791 per year, or $39.8 per hour.

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 8 days ago

Job description

Job Type
Part-time
Description
The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.
The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.
Key Responsibilities
Study Coordination & Execution
  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out
  • Schedule and conduct study visits in accordance with protocol requirements
  • Ensure proper informed consent is obtained and documented for all study participants
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents

Patient Care & Engagement
  • Identify, recruit, and screen eligible patients for clinical trials
  • Educate patients on study protocols, procedures, and expectations
  • Monitor patient safety and report adverse events in accordance with regulatory requirements

Data Management & Compliance
  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems
  • Perform source data verification (SDV) and ensure data integrity and completeness
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs

Collaboration & Communication
  • Serve as a liaison between investigators, sponsors, CROs, and internal teams
  • Support monitoring visits, audits, and regulatory inspections
  • Communicate effectively with cross-functional teams to ensure study milestones are met

Qualifications
Education & Experience
  • Bachelor's degree in life sciences, healthcare, or related field preferred
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus)
  • Experience working with clinical trial protocols and regulatory requirements preferred

Skills & Competencies
  • Strong organizational and time management skills
  • High attention to detail and accuracy in documentation
  • Excellent interpersonal and communication skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Proficiency in EDC systems and Microsoft Office Suite

Preferred Qualifications
  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA)
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas
  • Familiarity with clinical trial start-up and regulatory submissions

Salary Description
$53,000-$58,000

Apply