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Insurance Quality Assurance Jobs in Boca Raton, FL

B'Com Health

Quality Improvement Nurse

Hollywood, FL · On-site

... quality assurance / quality improvement activities. Responsible for assisting with training ... Paid Health, Dental, Life insurance * Paid Vacation and sick leave * 401k Retirement Plan w/Company ...

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Insurance Quality Assurance information

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$12

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$41

How much do insurance quality assurance jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for insurance quality assurance in Boca Raton, FL is $22.01, according to ZipRecruiter salary data. Most workers in this role earn between $16.63 and $23.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in insurance quality assurance, and why are they important?

To excel in Insurance Quality Assurance, a strong understanding of insurance products, regulatory compliance, and quality control methodologies is essential, often backed by relevant experience or a degree in business or insurance-related fields. Familiarity with audit management software, claims processing systems, and certifications such as Six Sigma or Certified Quality Auditor (CQA) is highly valuable. Attention to detail, analytical thinking, and strong communication skills help professionals identify issues and collaborate effectively with various stakeholders. These competencies are vital for ensuring that insurance operations meet industry standards and deliver reliable service to clients.

What does an insurance quality assurance professional do?

An Insurance Quality Assurance (QA) professional ensures that insurance processes, policies, and claims adhere to regulatory standards and company guidelines. They conduct audits, identify process improvements, and provide feedback to teams to enhance accuracy and efficiency. Their role helps minimize risks, ensure compliance, and maintain high service quality, ultimately protecting both the company and its customers.

What are popular job titles related to Insurance Quality Assurance jobs in Boca Raton, FL? For Insurance Quality Assurance jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Insurance Quality Assurance jobs in Boca Raton, FL look for? The top searched job categories for Insurance Quality Assurance jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Insurance Quality Assurance jobs? Cities near Boca Raton, FL with the most Insurance Quality Assurance job openings:
Insurance Quality Assurance jobs near you
Infographic showing various Insurance Quality Assurance job openings in Boca Raton, FL as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $45,775 per year, or $22 per hour.

Quality Assurance Coordinator (Clinical Research)

Research Centers of America

Hollywood, FL

$22.25 - $29.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 14 days ago

Job description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

Ensure that highest standards of data quality and study participant safety are maintained, as well as adherence to study protocols, CenExel SOPs, Site Working Practices (WPs), ICH GCP, Code of Federal Regulations, and IRB Guidelines.

Essential Responsibilities and Duties:

  • Assists the QA Manager in the development, implementation and follow-up of quality assurance programs including necessary or appropriate policies and guidelines.
  • Reviews follow-up monitoring visit reports, protocol deviation logs, and quality findings trackers for trend analysis.
  • Performs ongoing review of a percentage sampling of study inclusion/exclusion, study procedure records, and laboratory reports to ensure that they are conducted according to the protocol, applicable SOPs, ICH/GCP guidelines and federal regulations.
  • Performs quality review of initially created source documentation, including amendments, to ensure all protocol required procedures are present.
  • Prepares for internal and external audits and FDA inspections.
  • Attends staff meetings.
  • Attends site initiation visits as needed.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • 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.

Education/Experience/Skills:

  • Must be able to effectively communicate verbally and in writing in English and Spanish.
  • High school graduate or equivalent, Bachelors degree or equivalent preferred.
  • Minimum 1-2 years relevant experience in the clinical research industry.
  • Knowledge/Skills/Abilities: Must be self-directed and able to work with minimal supervision; Must have in depth knowledge of FDA regulations. GCP, and ICH guidelines; Able to take a flexible approach to shifting priorities; Able to manage multiple projects and responsibilities; Motivated to work consistently in a fast paced and rapidly changing environment; Must be detail oriented and have exceptional computer, organizational, and communication skills – both written and oral.
  • Must reflect the professional image of the company, upholding the company vision in actions, demeanor, and appearance.
  • Must be able to clearly communicate through written and verbal means with sponsors and staff.

 

Working Conditions

  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. On-site work arrangement.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

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