Director, Medical Development – MRD Breast Portfolio

Job not on LinkedIn

🕒 July 30

🏄 California – Remote

🏄 California – Remote

💵 $149.3k - $298.7k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 45%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 103 days.
• Jobs at this company usually fill in 24 days.
• Reposted once.

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Abbott

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1888

🏥 Healthcare

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare • Healthcare Insurance • Biotechnology

Abbott is a global healthcare company committed to advancing medical technologies and improving lives around the world. It offers a broad range of leading products in diagnostics, medical devices, nutrition, and branded generic medicines. Abbott's innovations such as the FreeStyle Libre glucose monitoring systems and BinaxNOW rapid antigen tests are transforming diabetes management and COVID-19 response. Through its partnerships and initiatives, Abbott aims to foster health equity, improve access to healthcare, and address critical health challenges like malnutrition and infectious diseases. Abbott is also dedicated to sustainability and social responsibility, striving to make life-changing technologies accessible and affordable.

📋 Description

• Develop the overall vision and strategy for Precision Oncology products, including recurrence score, therapy selection, molecular residual disease liquid biopsy, and digital pathology portfolios for breast cancer patients • Identify opportunities to expand indications for existing Precision Oncology products and develop new products within the biotech/pharma space • Collaborate with research and development, product, commercial, compliance, market access, and regulatory teams on commercialization strategy and product profiles • Serve as medical monitor on study teams and lead clinical protocols supporting product development, validation, and commercialization • Develop and adopt novel approaches for demonstrating clinical validation and utility • Engage medical and surgical and radiation oncology leaders to understand clinical questions and communicate the scientific validity and clinical utility of products • Lead external relationships with oncology leaders, academic institutions, cooperative groups, and research organizations • Identify investigators and sites for clinical trials • Initiate and lead external advisory boards involving pharma medical leaders, key opinion leaders, and other third parties • Review and interpret study results and translate them into evidence-based claims • Design and implement medical support for new or extended precision oncology tests and services • Provide oncology expertise and clinical insight throughout the lifecycle of multiomic tests and services • Account for scientific presentations and publications resulting from product development collaborations • Lead and participate in internal cross-functional program teams and working groups • Engage with the medical organization on team leadership practices, communications, interviews, team building, and culture • Identify biopharma partners for new product opportunities and indication expansion • Support the company’s Quality Management System policies and procedures • Travel up to 30% of working time, potentially including overnight/weekend travel

🎯 Requirements

• M.D. or D.O. in a related field • Completion of fellowship training or equivalent in medical oncology • Demonstrated expertise in molecular oncology • Demonstrated ability to lead cross-functional internal and external teams of professionals focused on complex, multi-faceted projects • Familiarity with laboratory analytical process development and biostatistics • Demonstrated ability to perform the essential duties of the position with or without accommodation • Authorization to work in the United States without sponsorship • 2+ years of experience in healthcare • Experience in oncology within the pharmaceutical or biotech industry with an emphasis on clinical or translational research • Experience working with various drug classes used in the management of breast cancer patients • Experience in the development of new oncology therapeutics and molecular diagnostics • Strong knowledge of FDA and Ex-U.S. regulatory documentation and processes

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