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Remote Audit Readiness Jobs (NOW HIRING)

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How much do remote audit readiness jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for remote audit readiness in the United States is $29.11, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $29.81 per hour, depending on experience, location, and employer.

What is the difference between Remote Audit Readiness vs Remote Compliance Analyst?

AspectRemote Audit ReadinessRemote Compliance Analyst
Required CredentialsCertifications like CPA, CIA, or ISO auditorCertifications such as CCEP, CISA, or compliance-specific credentials
Work EnvironmentPrepares organizations for audits, often involves documentation review and process assessmentMonitors and ensures ongoing compliance, analyzes policies and procedures
Employer & Industry UsageUsed by organizations preparing for external audits in finance, healthcare, or manufacturingEmployed by companies in regulated industries like finance, healthcare, or tech for compliance management

Remote Audit Readiness focuses on preparing organizations for audits through documentation and process review, while Remote Compliance Analyst continuously monitors and enforces compliance policies. Both roles require similar certifications and are vital in regulated industries, but their primary functions differ in audit preparation versus ongoing compliance management.

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Cities with the most Remote Audit Readiness job openings:

What are the most commonly searched types of Audit Readiness jobs?

The most popular types of Audit Readiness jobs are:

What states have the most Remote Audit Readiness jobs?

States with the most job openings for Remote Audit Readiness jobs include:

Infographic showing various Remote Audit Readiness job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 68% Full Time, 30% Part Time, and 1% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $60,553 per year, or $29.1 per hour.

Pharmaceutical Quality GVP Auditors Freelance/Independent (Consulting)

Remote

Advarra
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees

Part-time

Re-posted 7 days ago


Job description

If you're not already part of our Network, please register using the Expert Enrollment Form. https://advarra.my.site.com/experts/s/ Registration is required to be considered.
If you are in our network DO NOT fill out this form or click on the link.
Location
This role is open to candidates based in North America.
Company Information
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Company Culture
Our people--both employees and consultants-are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job Overview Summary
Advarra is seeking Good Pharmacovigilance Practice (GVP) Auditors to join our consultant network for North America -based projects. Auditors support compliance reviews across GVP clinical sites and vendors.
Job Duties & Responsibilities
  • Conduct Good Pharmacovigilance Practice (GVP) audits (planning, agenda, physical or remote audit, and report writing)
  • Evaluate investigator sites, CROs, and vendor compliance or qualification.
  • Prepare comprehensive audit reports detailing findings and root-causes.
  • Provide written audit reports in English.
  • If required will provide corrective actions support and present findings to QA leadership and stakeholders
  • Work collaboratively with clients to ensure quality standards.

Basic Qualifications
  • Minimum 10+ years of Clinical Quality Assurance and/or Good Pharmacovigilance Practice (GVP) experience.
  • Minimum 5+ years of Good Clinical Practices auditing experience.
  • Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
  • Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
  • Fluent English communication, verbal and written
  • Bachelor's degree

Preferred Qualifications
  • Strong interpersonal and client interaction skills.
  • Excellent analytical, problem-solving, communication, and report-writing skills.
  • Ability to work collaboratively across departments and interact with internal and external stakeholders.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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About Advarra

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Columbia, MD, US

Year founded

1983

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