What are the responsibilities and job description for the (MLR) Medical legal regulatory Compliance Specialist position at Ustech Solutions?
Title: MLR Compliance Specialist
Location: Irvine, CA
Duration: 10 months
Responsibilities:
- Operates as primary content approval contact for Global Sales Education/ Professional Education/ US Marketing.
- Prepares documents for VEEVA submissions; annotating and cross-checking references, tagging/linking/loading all related documents into the system.
- Serve as the liaison between the reviewers and content developers/SMEs to reach editorial solutions
- Immersion in relevant project claims matrices and references to become a Subject Matter Expert (SME) to proficiently and proactively navigate reviewer comments and make content recommendations that remedy compliance issues, if and when possible
- Ensures that all submissions accurately and consistently capture MLR comments and follow submissions through to approval.
- Create an internal tracking process that captures the current status of all projects routing for compliance review.
- Troubleshoots and guides submission workflow in challenging situations, supporting submission approval.
- Meets with reviewers to develop relationships, build rapport, and influence without authority.
- Develops best practices for content submission within Global Sales Education/ Professional Education/ US Marketing.
Qualifications:
- Minimum of a Bachelor's degree
- 3 years of (MLR) experience
Quality Assurance & Regulatory Compliance Specialist
JAC Recruitment -
Irvine, CA
Specialist - Premarket Regulatory Affairs
Applied Medical -
Rancho Santa Margarita, CA
Manager II, Medical Legal Regulatory Review
Welcome to the Tarsanet Internal Career Center! -
Irvine, CA
