Skip to main content

Flexible Work Arrangements

Compliance Key INC - Human Resource Training Online
Overview
Learn the regulatory requirements and legal ramifications of flexible working arrangements - flextime programs, job sharing, telecommuting, etc.
Why should you attend this webinar?
The air-tight rule of most companies in the past was that an employee was offered one of two types of positions: either full time or part time. As families are sharing child caring responsibilities, these employees are demanding something different. Employers have discovered that they can't just say "no" because another employer down the street is saying "yes". Companies saying "no" are finding themselves losing good valuable candidates to their competitors. And, laws such as the Americans with Disabilities Act are now requiring employers to consider flexible working arrangements if such does not impose an undue hardship on the organization. What are the different types of flexible working arrangements and the legal issues arising out of such arrangements? When do the benefits outweigh the risk of litigation? When does litigation outweigh the benefits?

This presentation will provide real life issues with solutions for your workplace. It will cover how to draft a good flexible working policy and what legal issues you should address.
Areas Covered in the Session:
  • Types of flexible working arrangements, including but not limited to job sharing, flex-time; compressed work weeks, etc.
  • Benefits to utilizing flexible work arrangements.
  • Problematic practical concerns when considering flexible work arrangements in your workplace.
  • Telecommuting as a flexible work arrangement (one of the most controversial)
  • Telecommuting as a reasonable accommodation under the ADA
  • Why attendance may not be considered an essential job function
  • Privacy and confidentiality concerns arising out of telecommuting arrangements
  • What a good telecommuting policy should include
Who can Benefit:
  • Human resource professionals
  • Inhouse counsel
  • chief financial officers
  • benefits specialists

Labels

Labels:
Location: United States

Comments

Post a Comment

Popular posts from this blog

HIPAA Compliance with the New Omnibus Rule: How to Pass an Audit to Avoid Penalties and Criminal Convictions

Compliance Key INC  -  H ipaa webinar                                           Jonathan P. Tomes Jonathan P. Tomes , J.D., is Keynote Speaker at Compliance key Inc. He is a health care attorney practicing in the greater Kansas City.   Webinar Id:   HIPHJPT001  2:30 PM PT | 03:30 PM ET    01/18/2018  Duration: 60 mins  Overview Before the HITECH Act, DHHS could audit covered entities for HIPAA compliance, but did not have to. With that Act, now the must audit those entities and business associates as well. In the first audits, the Phase I audits, DHHS came on site. The subsequent Phase II audits, however, were paper audits in which those audited had to provide documentation of their compliance. As yet, we do not know what form Phase III will take, but the necessary actions to prepar...
Post a Comment
Read more

HIPAA Compliant Fundraising Under New Rules - 2019

Compliance Key  -  H ipaa   Compliance Training HIPAA Compliant Fundraising Under New Rules - 2019 Joel Simon Joel Simon is one of the nation's leading experts on the fund raising aspects of HIPAA. Joel has been a member of the Maryland bar for 30 years, and his professional experience includes work as the assistant general counsel of a community hospital. Joel is an editor of "Fundraising Under HIPAA" published by the Association of Fundraising Professionals. He has lectured on Fund Raising under HIPAA to national audiences since the original HIPAA regulations were first proposed 17 years ago. Read More Overview Not-for-Profit organizations that are governed by HIPAA often need or want to fund raise from their patients, clients, or families. What protocols should be in place to maximize philanthropic opportunities under HIPAA? What compliance measures need to be in place and assessed to properly use protected health information for fund raisi...
Post a Comment
Read more

Classifying Medical Devices in US and EU

Compliance Key INC  -  Healthcare Compliance Webinars Overview The Food and Drug Administration (FDA) has established classifications for approximately 1,700 different generic types of devices and grouped them into 16 medical specialties referred to as panels. Each of these generic types of devices is assigned to one of three regulatory classes based on the level of control necessary to assure the safety and effectiveness of the device.The determination process, how you apply the classification process to your device, is complex and requires several levels of analysis to make the proper device classification. Proper medical device classification is the fundamental first step in submitting your device for approval anywhere in the world. This webinar will detail the medical device classification process for the United States through the FDA and will overview the very complex process for medical device classification within the EU. Specifically, this webinar will provid...
Post a Comment
Read more