Compliance Support Associate

Posted 4hrs ago

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Job Description

Agiloft & ComplianceWire Support Associate providing operational support for compliance workflows in regulated life sciences. Requires experience with AgileLoft and ComplianceWire platforms.

Responsibilities:

  • Provide day-to-day support for AgileLoft users, including content routing, workflow management, and issue resolution
  • Assist with setup and maintenance of review workflows, user roles, and permissions
  • Troubleshoot submission, approval, and annotation issues within MLR processes
  • Support content lifecycle management, including versioning, tagging, and archiving
  • Partner with Marketing, Medical, and Legal teams to ensure timely review cycle completion
  • Administer and maintain ComplianceWire training assignments, curricula, and user records
  • Support onboarding/offboarding activities and training compliance tracking
  • Troubleshoot user access, training completion, and reporting issues
  • Generate and distribute compliance reports for audits and internal stakeholders
  • Ensure training records align with regulatory and audit requirements (GxP, FDA, etc.)
  • Serve as first-line support for system-related inquiries and escalate issues as needed
  • Maintain system documentation, SOPs, and job aids
  • Support data integrity, validation activities, and audit readiness efforts
  • Collaborate with IT, QA, and vendors for system enhancements and issue resolution
  • Monitor system performance and proactively identify improvement opportunities

Requirements:

  • Bachelor’s degree in Life Sciences, Business, IT, or related field
  • 2+ years of experience supporting AgileLoft, ComplianceWire, or similar platforms (MLR/PRC tools and LMS systems)
  • Strong understanding of content review processes and training compliance in regulated environments
  • Experience with user support, ticketing systems, and issue troubleshooting
  • Proficiency in Excel and reporting tools
  • Strong attention to detail and documentation skills
  • Ability to work PST hours and collaborate with cross-functional teams
  • Experience in pharmaceutical, biotech, or medical device industries (preferred)
  • Familiarity with GxP, FDA regulations, and audit readiness processes (preferred)
  • Experience with Veeva PromoMats, Veeva Vault, or other MLR systems (preferred)
  • Knowledge of data governance and compliance frameworks (preferred)
  • Exposure to validation processes (CSV) or system release management (preferred)