Intervention Specialist

Invo Healthcare Associates Inc Cincinnati , OH 45201

Posted 3 months ago

Best Practices. Best Careers. Best Outcomes for Children. The Invo-Progressus team has incredible full and part-time career opportunities available for Intervention Specialists in Cincinnati, OH to provide services in a K-12 school program. Call 800-892-0640 to speak with a dedicated Career Services Manager!

For more than twenty years, Invo-Progressus has been providing therapeutic services that create better outcomes for children. The Invo-Progressus team is comprised of some of the nation's most talented and influential education and therapy leaders all of whom have a keen understanding of how to meet the unique needs of school districts, children and families and help them succeed. We are committed to helping children and families, school leaders and clinicians achieve success.

Requirements:

  • Current Mild to Moderate Intervention Specialist Licensure in Ohio

  • Alternative Resident Educator License ODE Certification

  • Experience working in school programs or with pediatric populations is preferred

  • Plan and deliver instruction to identified students in the classroom or intervention in small groups or 1:1 as needed to help students meet IEP goals.

  • Work closely with the classroom teacher in making sure student needs are met, goals and objective per child's educational plan are taught and provisions are followed

  • Assist with designing behavior plans for students who have behavioral challenges that interfere with their learning or others' learning

  • Assist the Team with designing intervention and monitoring RTI for students who are struggling, but not identified for special education services

  • Maintain appropriate records, progress reports and compliance reporting

  • Work in coordination with school personnel and parents to develop appropriate programs for eligible students

  • Ability to effectively communicate with teachers, administrators, and parents

  • Ensure all services are performed in accordance with state laws and regulations

  • Perform other Intervention Specialist duties/responsibilities required by the Program and within the scope of licensure and/or certification

Benefits:

  • Competitive compensation with flexible pay options

  • Comprehensive Benefits Package (Medical/Dental/Vision Coverage, 401(k) Retirement Saving Plan with a discretionary company match)

  • Flexible Spending Plan for medical and dependent coverage

  • Professional Liability Coverage

  • Licensure reimbursement

  • Annual Professional Development stipend

  • Professional membership stipend

  • Unlimited CEUs through the Progressus Pathways Learning Center

  • Unparalleled mentoring and support

  • Many More!

INVO is an equal opportunity employer and conducts all business activities (e.g., recruitment, hiring, assignment, conditions of employment, compensation, benefits, training, promotion, discipline and termination) without regard to race, color, religion, national origin, ancestry, age, marital status, sex, sexual orientation, pregnancy, gender identity or expression, genetic information, disability, veteran status, military and veteran status, or any other protected characteristic under applicable federal, state and local law.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Senior Regulatory Affairs Specialist

Johnson & Johnson

Posted 4 days ago

VIEW JOBS 1/15/2020 12:00:00 AM 2020-04-14T00:00 Ethicon, a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Senior Regulatory Affairs Specialist to be located in Cincinnati, OH. Ethicon develops and markets advanced medical devices for minimally invasive and open surgical procedures. The company focuses on procedure enabling devices for the interventional diagnosis and treatment of conditions in general and bariatric surgery, as well as gastro-intestinal health, gynecology and surgical oncology. The Senior Regulatory Affairs Specialist will conduct a refreshingly wide range of regulatory activities necessary for the timely preparation, writing and filing of 510(k) Pre-market Notifications, European submissions, and support international product registrations. The role will manage the global regulatory aspects of new product development and supply chain distribution for specified products with minimal direction from management. In this role, you will: * Prepare and submit documents necessary to gain US and international regulatory approvals / clearance to place new or modified products into worldwide commercial distribution * Stay continually aware of new product development activities through ongoing communication with Marketing and Research & Development departments, in addition to supporting portfolio management * Provide expertise, make recommendations and give regulatory direction as an integral member of new product development team * Provide regulatory support to medical affairs, supply chain teams, analyze technical reports, and review advertising and promotional materials * Communicate with department members, government agencies and a host of individuals outside the company in a professional, decisive, and articulate manner * Make recommendations and provide guidance to marketing, product development, technical writers, and package engineering regarding label content Qualifications * A minimum of a Bachelor's degree in life science, engineering, medical/scientific writing, public health administration or a related area is required. * An advanced degree in a technical, medical, or business area is an asset. * RAC (Regulatory Affairs Certification) by Regulatory Affairs Professional Society is preferred. * A minimum of 4 years of successful experience in a regulated healthcare environment (device, pharmaceutical, biologics company, etc.) is required. * Experience with US regulatory submissions, such as 510(k), NDA, or PMAs, is required. * It is preferred that this individual has experience with or exposure to international regulatory requirements. * Device submissions experience is preferred. * Experience with IDEs (Investigational Device Exemptions), PMA Supplements and/or Annual reports, Clinical Trial Dossiers (CTD), Design Dossiers/Renewals, Technical Files, and/or Clinical Trials is an asset. * Broad based experience across various disciplines is useful. * This position will be located in Cincinnati, Ohio and may require up to 10% travel. Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. Primary Location United States-Ohio-Cincinnati- Organization Ethicon Endo Surgery Inc (6041) Job Function Regulatory Affairs Requisition ID 5083200113 Johnson & Johnson Cincinnati OH

Intervention Specialist

Invo Healthcare Associates Inc