Director, Medical Development, Precision Oncology

🔥 1 minute ago

🏄 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 0%

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.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

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 Exact Sciences’ Precision Oncology products, including Oncotype DX, OncoExTra, therapy selection, and molecular residual disease portfolios • Identify opportunities to expand indications for existing Precision Oncology products and develop new products within the pharma space • Provide medical expertise for commercialization strategies and product profiles for new products and services • Serve as medical monitor on study teams and lead clinical protocols supporting product development, validation, and commercialization • Engage oncology leaders to understand clinical questions, identify clinical tool needs, and communicate the scientific validity and clinical utility of products • Lead scientific presentations and publications resulting from product development collaborations • Provide oncology expertise and clinical insight to cross-functional teams throughout the lifecycle of genomic tests and services • Build and lead internal and external collaborations with academic oncology leaders, cooperative trial groups, research organizations, investigators, and clinical trial sites • Initiate and lead external advisory boards involving pharma medical leaders, key opinion leaders, and other third parties • Review and interpret key study results and lead reporting • Design and implement medical support for new or extended precision oncology tests and services • Lead and participate in cross-functional teams spanning business development, research and development, pathology, clinical laboratory operations, biostatistics, clinical affairs, medical affairs, regulatory, market access, and commercial functions • Identify pharma partners for new product opportunities and indication expansion • Support continuous improvement of team leadership practices, communications, interviewing, team building, and Precision Oncology culture • Apply analytical, communication, prioritization, collaboration, and quality-focused practices • Support and comply with Quality Management System policies and procedures • Maintain regular and reliable attendance • Travel as required

🎯 Requirements

• M.D. or D.O. in a related field as outlined in the essential duties • Completion of fellowship training or equivalent in 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 • Preferred: 2+ years of experience in healthcare • Preferred: Experience in oncology within the pharmaceutical or biotech industry with an emphasis on clinical or translational research • Preferred: Experience working with checkpoint inhibitor therapies • Preferred: Experience in the development of new oncology therapeutics and molecular diagnostics • Preferred: Strong knowledge of FDA and Ex-U.S. regulatory documentation and processes • Ability to act with an inclusion mindset and model these behaviors for the organization • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day

🏖️ Benefits

• Travel up to 30% of working time may include overnight/weekend travel • Equal Opportunity Employer protections for Minorities/Women/Individuals with Disabilities/Protected Veterans

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume