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$15K

$241.3K

$387K

How much do compliancewire on jobs pay per year?

As of Jul 14, 2026, the average yearly pay for compliancewire on in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What is the difference between Compliancewire On vs Compliance Analyst?

FeatureCompliancewire OnCompliance Analyst
Primary RoleTraining management and compliance trackingMonitoring and analyzing compliance data
Required CredentialsTypically no specific certifications requiredOften requires certifications like CCEP or CAMS
Work EnvironmentOnline platform used across industriesOffice or remote, focused on compliance audits
Industry UsageUsed by organizations for training complianceEmployed by compliance departments in various sectors

Compliancewire On is a learning management system for training compliance, while a Compliance Analyst focuses on analyzing compliance data and ensuring regulatory adherence. Both roles are integral to organizational compliance but serve different functions within the compliance ecosystem.

More about Compliancewire On jobs
What cities are hiring for Compliancewire On jobs? Cities with the most Compliancewire On job openings:
What states have the most Compliancewire On jobs? States with the most job openings for Compliancewire On jobs include:
What job categories do people searching Compliancewire On jobs look for? The top searched job categories for Compliancewire On jobs are:
Compliancewire On jobs near you
Infographic showing various Compliancewire On job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 4% As Needed, 93% Part Time, and 1% Nights. Highlights an 100% Hybrid job distribution, with an average salary of $241,295 per year, or $116 per hour.
Veeva QualityDocs & ComplianceWire Administrator (Consultant)

Veeva QualityDocs & ComplianceWire Administrator (Consultant)

Adeptsource

Manhattan, NY • On-site, Remote

Full-time

Re-posted 25 days ago

Job description

Title: Veeva QualityDocs & ComplianceWire Administrator (Consultant)
Location: Remote
Duration: Consultant / Contract
We are seeking an experienced Veeva Administrator Consultant to support and manage our Veeva QualityDocs (QDocs) and ComplianceWire LMS platforms. This consultant will act as a subject matter expert, owning day-to-day administration, user support, document lifecycle management, and training compliance activities.
The ideal candidate has deep, hands-on experience in GxP-regulated environments and is comfortable working independently while partnering closely with Quality, Regulatory, and Clinical Operations teams in a fast-moving clinical-stage biotech setting.
**Must have extensive experience with both Veeva QualityDocs (QDocs) and ComplianceWire LMS.
Key Responsibilities:
Veeva QualityDocs (QDocs) Administration
  • Serve as SME and primary administrator for Veeva QualityDocs.
  • Configure and manage document lifecycles, workflows, templates, and metadata.
  • Support document authoring, review, approval, issuance, periodic review, and archival.
  • Manage user roles, permissions, and access controls.
  • Perform system configuration, troubleshooting, and issue resolution.
  • Support audits and inspections by ensuring system compliance and documentation readiness.
  • Develop SOPs, work instructions, and best practices related to document management.
ComplianceWire LMS Administration
  • Administer ComplianceWire LMS including course assignments, curricula, and training matrices.
  • Manage user accounts, roles, and organizational structures.
  • Track and report training compliance and completion metrics.
  • Support onboarding and role-based training programs.
  • Configure and maintain learning paths and certification requirements.
Required Qualifications
  • SME-level experience administering Veeva QualityDocs (QDocs).
  • Strong hands-on experience with ComplianceWire LMS administration.
  • Experience supporting GxP-regulated environments (biotech, pharma, medical device).
  • Knowledge of quality systems, document control, and training compliance processes.
  • Experience with system configuration, workflows, and access controls.
  • Strong troubleshooting and problem-solving skills.
  • Ability to work independently in a remote, fast-paced startup environment.
  • Excellent communication and stakeholder management skills.

Apply