Analyst, Regulatory Programs Position Available In Norfolk, Massachusetts

Analyst, Regulatory Programs Foxboro, MA • Customer Support & Training
Job Type
Full-time
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.