Director of Clinical Affairs Endoluminal

Added
8 days ago
Type
Full time
Salary
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Related skills

gcp regulatory affairs clinical trials mdr iso 14155

📋 Description

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

🎯 Requirements

  • Advanced degree such as M.D, MS or PhD in scientific/bioengineering field with minimum 8 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
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