Staff Clinical Engineer, Interventional Oncology (into)

Johnson & Johnson MedTech

Cambridge, Massachusetts, United States of America
$109,000.00 - $174,800.00; not specified; vacation...
Hybrid (3 days onsite)
Clinical procedure development
Intratumoral therapy procedures
Risk identification and mitigation
Johnson & Johnson MedTech is seeking a Staff Clinical Engineer for their Interventional Oncology team, responsible for bridging clinical workflows with medical technology development to enhance cancer treatment. The position requires a blend of technical expertise in healthcare innovation and collaborative skills to lead clinical trial procedures, with a focus on patient-centered solutions

Job Summary

  • Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.
  • The Interventional Oncology (INTO) group, a cross-sector initiative at J&J, brings together the pharmaceutical and medical device expertise with the aim to meaningfully alter the course of cancer and improve survival.
  • As a Clinical Engineer, you will lead the development of clinical procedures that support clinical trials critical to the success of INTO’s cross-sector Development Teams.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Staff Clinical Engineer for their Interventional Oncology team, responsible for bridging clinical workflows with medical technology development to enhance cancer treatment. The position requires a blend of technical expertise in healthcare innovation and collaborative skills to lead clinical trial procedures, with a focus on patient-centered solutions.

Salary

$109,000.00 - $174,800.00; Not specified; Vacation –120 hours per calendar year, Sick time - 40-56 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240/40 hours, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours, Military Spouse Time-Off – 80 hours

Skills & Requirements

Must-have

  • Clinical procedure development
  • Intratumoral therapy procedures
  • Risk identification and mitigation
  • Voice of customer studies
  • Cross-sector collaboration

Nice-to-have

  • Human-centric design
  • Medical standards understanding
  • Scientific conferences attendance
  • Teamwork and inclusion
  • Problem-solving skills

Key Requirements

  • Bachelor's degree in technical field with biology understanding
  • 5+ years healthcare/pharma/medical device experience
  • 3+ years product development experience
  • Experience with human factors/usability studies
  • Experience with risk identification/mitigation
  • Experience facilitating physician interaction/VoC
  • Experience with experiment development
  • Experience with customer/user requirements development
  • Experience with instruction for use development
  • Ability to travel 20-40%

Work Rights

Not specified

Tailored Resume

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