Job Description

The Analyst, Regulatory Programs will serve as a subject matter expert to customers and internal staff by providing expertise to the complexities of their aligning regulatory programs.

As a member of our Organizational Development team, your job would involve:

• Participating in calls internally and with customers to provide regulatory guidance and expertise
• Reading and collaborating to interpret and operationalize CMS Proposed and Final Rules
• Collaborating with Development and stakeholders to evaluate the impact of product requirements and workflows for successful attestation
• Participating in Regulatory related cross divisional meetings and collaborations as needed
• Coordinating and contributing to the development and documentation of the Regulatory Best Practices. This includes providing guidance to ensure workflows meet the requirements
• Scheduling meetings as needed to optimize communication, manage project plans, and follow through with action items
• Collaborating to establish and evaluate workflows for accurate report data capture
• Participating in report testing and creation of patient test data
• Publishing Best Practices to the Regulatory pages, adhering to established guidelines
• Updating the Best Practice Change Log with accurate reflection of edits
• Developing internal and external educational resources. This can include, but is not limited to, written documentation and articles, e-learning tutorials, in-person presentations, webinars, and hosting customer round tables
• Collaborating with counterparts to evaluate and implement any needed redesign of Regulatory pages to improve customer and internal communication and educational resources
• Facilitating Regulatory Focus Groups as needed to evaluate documentation, communications, and education based on customer needs and feedback
• Responding to customer and internal questions submitted through the Regulatory Mailbox
• Assisting with customer regulatory support/issue management
• Participating in industry education/forums to build and maintain knowledge of regulatory programs
• Promoting and adhering to the Quality Management System guidelines and policies.

Requirements

• Bachelor’s or associate degree preferred and/or 2-3 years applicable work or military experience
• Strong interpersonal and collaborative skills
• Strong written and verbal communication skills
• Excellent organizational skills and proven ability to meet deadlines, prioritize, and manage multiple tasks or projects at a time
• Excellent customer service skills and desire to promote service excellence
• Strong analytical, problem-solving, and project management skills
• Independent worker who takes initiative and who requires minimal supervision
• Experience with MEDITECH clinical applications and related workflow is desirable
• Presentation and teaching experience highly desirable.

Hiring salary range: $60,000- $72,000 per year.

Actual salary will be determined based on an individual's skills, experience, education, and other job-related factors permitted by law.

MEDITECH offers competitive employee benefits including but not limited to health, dental, & vision insurance; profit sharing trust and 401(k); tuition reimbursement, generous paid time off, sick days, personal time, and paid holidays.

This is a hybrid role which includes a blend of in-office and remote work as designated by the management team.

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. MEDITECH will not sponsor applicants for work visas.

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