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Part Time Clinical Research Coverage Analyst Jobs

IQVIA

Clinical Research Coordinator

Sioux Falls, SD

$35 - $42/hr

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 ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$35 - $42/hr

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 ...

IQVIA

Clinical Research Coordinator

Jefferson City, MO

$35 - $42/hr

... analytics, technology solutions, and clinical research services, dedicated to driving healthcare ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

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

Main Line Health

Clinical Research Coord II

Wynnewood, PA · Hybrid

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... coverage and responsibilities Location: Lankenau Medical Center Requires the ability to travel ...

IQVIA

Clinical Research Coordinator

Marietta, GA

$35 - $42/hr

... analytics, technology solutions, and clinical research services, dedicated to driving healthcare ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Union, SC

$35 - $42/hr

... analytics, technology solutions, and clinical research services, dedicated to driving healthcare ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Main Line Health

Clinical Research Coord I

Wynnewood, PA · On-site

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... coverage and responsibilities Location: Clinical research program focused at Lankenau Medical ...

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Part Time Clinical Research Coverage Analyst information

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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.
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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.

Clinical Research Physician - Psychiatrist (Part time)

Alcanza Clinical Research

Deland, FL • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 12 days ago

Job description

Clinical Research Physician - Psychiatrist (Part time)
Department: Operations
Employment Type: Part Time
Location: Accel Research Sites - DeLand, FL
Reporting To: Diana Toney
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Skills, Knowledge and Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Board certification in Psychiatry is required.
Required Skills:
  • Clinical skills and clinical procedures based in area of specialty.
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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