Sr. Director, Clinical Affairs - Endoluminal

Added
5 hours ago
Type
Full time
Salary
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Related skills

gcp regulatory affairs medical devices clinical research mdr

๐Ÿ“‹ Description

  • Play a lead role in the development of the company's clinical and scientific strategies, including
  • Accountable for development and execution of clinical study plans to conform to applicable
  • Responsible for providing strategic guidance to global clinical evidence strategy for the
  • Responsible for cross functional partnerships with various key functions within the organization to
  • Highly skilled at translating strategic, corporate and technical content into clear evidence of
  • Drive the development and implementation of clinical research strategies to meet business goals and

๐ŸŽฏ Requirements

  • Advanced degrees such as M.D, MS or PhD in scientific/bioengineering field with 8-12 years of
  • Previous experience assisting with the development of scientific strategies for IDE, pre-market
  • Possess knowledge of Good Clinical Practice and 21 CFR medical device regulations, ISO 14155, Med
  • Solid knowledge and background of clinical trials, study design and formal ICH/GCP knowledge and
  • Proven track record of leadership by example and developing high performing teams
  • Excellent ability to interact with physicians and other professionals inside and outside the

๐ŸŽ Benefits

  • Market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity.
  • Equal Opportunity Employer
  • Reasonable accommodations for qualified individuals with disabilities
  • Preference to candidates who do not reside in certain states
  • Potential for export license or Technology Control Plan
  • Vaccination requirement may apply
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