Principal Clinical R&D Advisor

2 weeks ago


Santa Clara, California, United States Abbott Laboratories company Full time

Job Description:

Abbott is a renowned global healthcare organization dedicated to enhancing people's quality of life across all life stages. With a diverse portfolio of innovative technologies in diagnostics, medical devices, nutritionals, and generic medicines, Abbott has a wide-reaching impact on healthcare worldwide.

Position:

Principal Clinical R&D Advisor

About Working at Abbott:

Abbott offers a fulfilling work environment where you can make a meaningful impact, develop professionally, prioritize self-care and family, and embrace your authentic self. By joining Abbott, you gain access to:

  • Career advancement opportunities in a global company to nurture your professional growth and aspirations
  • Comprehensive medical coverage through the Health Investment Plan (HIP) PPO for employees*
  • A robust retirement savings plan with generous employer contributions
  • Tuition reimbursement, Freedom 2 Save student debt program, and FreeU education benefit for pursuing a bachelor's degree affordably and conveniently
  • Recognition as a top employer in numerous countries and among the most admired companies globally, as recognized by Fortune
  • A commitment to diversity, supporting working mothers, female executives, scientists, and creating a positive workplace environment

Opportunity Overview:

Abbott Vascular specializes in providing innovative, minimally invasive, and cost-effective solutions for vascular disease treatments. The product range includes drug-eluting stents, guide wires, catheters, and peripheral stents, among others.

Position Summary:

Based in Santa Clara, CA, the Principal Clinical R&D Advisor role involves offering clinical expertise and guidance across various stages of product development to ensure informed decision-making related to manufacturing, quality, and patient safety.

Key Responsibilities:

  • Contribute clinical insights to product development processes, including bench testing, in-vitro/in-vivo evaluations, and developing new testing methods
  • Create clinical performance evaluation plans to gauge physician acceptance and product performance
  • Draft Device Instructions For Use (IFU)
  • Participate in risk analysis and product action processes to assess and mitigate potential risks associated with device use
  • Support decision-making on product recalls or actions based on clinical feedback and expertise
  • Build a strong network to facilitate project completion
  • Mentor and guide junior staff, set project goals, and influence technical and business solutions
  • Apply innovative methods to resolve problems effectively

Qualifications:

Required:

  • Bachelor's degree
  • Minimum 7 years of relevant work experience with a focus on the specified functional area
  • RT, RN, or RCIS certification or degree
  • Recent catheter lab experience (coronary + endovascular ideal)
  • Strong business acumen and proficiency in quality system environments
  • Willingness to travel up to 25-30%, including internationally

Preferred:

  • Training in catheter lab product testing, writing skills, and interpersonal communication
  • Experience with medical device quality systems and regulatory processes
  • Familiarity with fluoroscopy unit operation and sterile environments
  • Proficiency in Microsoft Office applications for data analysis and presentations

About Abbott:

Discover diverse career opportunities at Abbott, a leading employer committed to helping individuals shape their future and lead fulfilling lives. As an Equal Opportunity Employer, Abbott prioritizes employee diversity and growth.



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