Principal Scientist, Clinical Research (robotics & Digital Solutions) - Medtech Surgery

Johnson & Johnson

Santa Clara, California, United States of America
$134,000.00 - $231,150.00 py
Onsite
Global evidence generation strategies
Design clinical trials
Real-world evidence implementation
Develop and deliver global evidence generation strategies (pre- and post-market approval studies, investigator initiated, real world evidence) aligned to the needs of R&D, Regulatory, and Commercial

Job Summary

  • Develop and deliver global evidence generation strategies (pre- and post-market approval studies, investigator initiated, real world evidence) aligned to the needs of R&D, Regulatory, and Commercial.
  • Develop network with key surgeons in US, EU, and APAC to assist in execution of Robotic Surgery clinical trials for registration in all regions.
  • Support clinical scientific discussions with regulatory agencies/notified bodies to drive support of the clinical and regulatory strategy, including proposed clinical investigations.

Matching Summary

Develop and deliver global evidence generation strategies (pre- and post-market approval studies, investigator initiated, real world evidence) aligned to the needs of R&D, Regulatory, and Commercial.

Salary

$134,000.00 - $231,150.00

Skills & Requirements

Must-have

  • Global evidence generation strategies
  • Design clinical trials
  • Real-world evidence implementation
  • Network with key surgeons
  • Interpret and disseminate evidence
  • Support clinical scientific discussions with regulatory agencies

Nice-to-have

  • Innovative business development assessment
  • Influence and lead teams
  • Build internal relationships
  • Develop external partnerships

Key Requirements

  • Bachelor’s degree in Biological Science, Engineering, or related field
  • Advanced Degree (Master’s or Ph.D.) strongly preferred
  • 8+ years of related scientific/technical experience
  • Experience in clinical research science and processes
  • Experience in product development processes
  • Experience in global clinical trial regulations
  • Proven track record in clinical programs
  • Experience working in Robotics strongly preferred
  • Experience in support of global regulatory submissions preferred
  • Clinical Monitoring experience highly desired

Work Rights

Not specified

Tailored Resume

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