Edwards Lifesciences Corp

Manager, Physician Training - Mid West Region

Edwards Lifesciences Corp$126K — $178K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree or 8 years equivalent clinical experience required
  • Registered Nursing (RN) license, Registered Respiratory Therapist (RRT) certification, or Registered Diagnostic Cardiac Sonographer (RDCS) preferred
  • Strong organizational and project management skills
  • Proficiency in Microsoft Office Suite
  • Excellent documentation and communication skills
  • Extensive knowledge of regulatory and compliance requirements
  • Attention to detail and ability to manage competing priorities

Responsibilities

  • Lead clinical study execution within the Business Unit
  • Develop and standardize training curriculum for specialists and physicians
  • Collaborate with internal and external stakeholders to ensure compliance
  • Create training content on best practice topics
  • Evaluate and train team members on training processes
  • Maintain an audit-ready environment for regulatory compliance
  • Manage electronic documentation processes for training

Benefits

  • Competitive salaries and performance-based incentives
  • Wide variety of benefits programs for employees and their families
  • Opportunities for professional development and training
Full Job Description

Play a critical role in assigned Business Unit clinical study execution including leading the internal specialist training program and maintain an audit ready en

How you will make an impact:

  • The Manager Physician Training THV will play a critical role in assigned Business Unit clinical study execution including leading the internal specialist training program and maintain an audit ready environment by ensuring compliance with all physician and training procedures, maintain drive high levels of accuracy and compliance

  • Lead and drive the Business Unit training program through curriculum execution, standardization, content development, SME resource management, and documentation to ensure study compliance, as it relates to physician and clinical specialist training, in accordance with regulations and corporate processes.

  • Maintain regular contact and collaborate with partner BU clinical teams, cross BU partners, consultants, customers and network appropriately with relevant stakeholders.

  • Develop content as it relates to specialist training topics for best in class practices as they relate to required non-procedural knowledge.

  • Train and evaluate the quality of team members execution of specialist and physician training processes and documentation as it relates to physician and clinical specialist training.

  • Responsible for maintaining an audit ready environment for all aspects of regulatory and non-regulatory audits as it relates to training (e.g., conducting training, identifying SMEs, ensuring the collection of required documentation.) Lead assessment of teams’ compliance to GSOPs, work instructions, protocols, LMS and regulatory requirements.

  • Lead audit preparation efforts for BU including team education, process development, timeline management, communication and implementation.

  • Identify, acquire, develop and maintain programs used for electronic documentation records and processes (e.g., Trifecta, Veeva Vault, Litmos) for both internal and external training.

  •  Strategically develop and lead the delivery of training programs for BU training on best practices, trends, regulatory requirements and published guidance, policy and procedure updates, etc.

  • Review and contribute to the development of policies, physician training documentation, clinical specialist training, and other documents to be audit ready.

  • Manage, leverage and communicate detailed metrics reporting including training compliance and employee training dashboards to drive compliance.

  • Assess, manage and ensure the resolution of audit findings and protocol deviations while developing priorities and strategies to drive compliance.

  • Lead the development, continuous improvement and streamlining of processes and procedures to ensure efficiency and accuracy in accordance with regulatory and company requirements.

  •  Other incidental duties: Lead resources tasked with training logistics.

What you’ll need (required):

  • Bachelor's Degree or Equivalent 8 years experience of work experience with strong clinical background or equivalent work experience based on Edwards criteria Required

  • Up to 50% travel nationwide required This will include Midwest travel as much as possible but may expand beyond during busy seasons.

What else we look for (preferred):

  • Completion of an accredited program with a Registered Nursing (RN) license, Registered Respiratory Therapist (RRT) certification, Registered Diagnostic Cardiac Sonographer (RDCS)

  • Proven successful organizational and project management skills

  • Proven expertise in Microsoft Office Suite

  •  Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives

  • Extensive knowledge of own area within the organization while contributing to the development of new concepts, techniques, and standards

  • Extensive understanding of related aspects of clinical therapeutic areas

  • Extensive knowledge of regulatory, compliance, and AdvaMed requirements

  • Strict attention to detail

  • Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization

  • Ability to manage competing priorities in a fast paced environment

  • Must be able to work effectively within a specific area with cross-functional team, marketing peers and leaders and managing needs and messaging to upper management

  • Maintain a strong relationship with the regional sales team, clinical specialists, and training to ensure effective and optimal integration of efforts.

  •  Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For Illinois, the base pay range for this position is $126,000 to $178,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).Applications will be accepted while this position is posted on our Careers website.  

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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