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Invitae

Medical Affairs Director (US) - Partnerships, Oncology

Remote

Invitae (NYSE: NVTA) is a leading medical genetics company trusted by millions of patients and their providers to deliver timely genetic information using digital technology. We aim to provide accurate and actionable answers to strengthen medical decision-making for individuals and their families. Invitae's genetics experts apply a rigorous approach to data and research, serving as the foundation of their mission to bring comprehensive genetic information into mainstream medicine to improve healthcare for billions of people.

The Medical Affairs Director  - Partnerships, Oncology is responsible for supporting Invitae’s business development teams (US and International) by providing the necessary scientific expertise and guidance to various cross-functional teams relevant to complex oncology services.  Specifically, this person is the primary internal subject matter expert for oncology diagnostics (including minimal residual disease (MRD) testing services for solid tumor and hematological cancers, exome/genome sequencing technologies and ctDNA sequencing for translational research & therapy selection, and comprehensive germline next-generation sequencing panel), pharmaceutical clinical trial development, and regulatory requirements. Additionally, this person serves as an internal resource, as well as an externally-facing thought leader, establishing Invitae’s differentiated offerings. Furthermore, this position provides the necessary support for Invitae’s other commercial teams responsible for developing products and services that enhance our biopharma partnerships.

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The individual in this position is also the Directly Responsible Individual (DRI) serving as the single interface for the development of novel oncology diagnostics to meet the needs of our commercial partners. The DRI works with a variety of medical, development, and commercial stakeholders to collect the appropriate details and expertly synthesize the necessary requirements and provide an actionable set of decisions that the Product Development team can use. This individual is also responsible for providing insights to ensure the sound incorporation of Invitae products into the partner’s clinical trial protocol design. In addition, this individual will support research collaborations with biopharma collaborators, publishing papers, and supporting campaigns around publications and collaborations. 

This individual has extensive expertise in research design, methodology, and various technologies and is able to help guide study design for both internally-driven studies and externally-led collaborations. They will also have the necessary vision and point of view to independently drive Invitae’s scientific strategy including identifying relevant conferences and speaking opportunities and publication topics. This person is knowledgeable about competitors and peers in oncology genomic diagnostics and the oncology drug development landscape and is able to speak with scientific credibility about the strengths and limitations of different diagnostic assays, clinical trial design, as well as the business and scientific implications involved in different use cases in the early and late stage clinical and post-marketing setting.

What you'll do:

  • Providing direct medical information support to Invitae’s business development teams (US and International) in way of:
    • Expertise in the competitive landscape of ctDNA applications and MRD
    • Participating in introductory/pitch calls, assisting with RFPs and deal negotiations, due diligence, etc. 
    • Ongoing client support related to assay/methodology, clinical reporting, clinical trial protocol design, abstracts/posters/conferences, etc. 
    • Medical support in relation to contracts, program changes, legal proceedings
  • In collaboration with the Business Development Team, prepare strong RFPs for partnership opportunities
  • Obtain and route feedback on biopharma partnerships-related product improvements to development teams
  • Regularly conduct research in collaboration with business partners to support Invitae’s goals and establishing scientific credibility for Invitae
  • Author or co-author internally and externally led publications involving Invitae’s oncology products
  • Responsible for scientific review and approval of public-facing materials regarding oncology testing including publications, abstracts, press releases, social media posts, etc.
  • Speaking publicly at conference, webinars, and panels
  • Serve as a genetics expert in oncology genetic testing (MRD, somatic and inherited oncology genetic testing). Experience in genetic diagnostic and/or pharmaceutical clinical trial design preferred

What you bring:

  • A clinical or scientific advanced degree with >5 years of postgraduate experience. Clinically board certified preferred.
  • Experience with oncology diagnostics or therapeutics mandatory; experience with clinical trial design and regulatory filings preferred.
  • Visible stature in the research community through participation in academic and professional societies and engagement in public speaking opportunities
  • Experience with peer-reviewed research publications as a co-author on a variety of manuscripts and abstracts
  • Ability to be onscreen for virtual meetings with clients, in an undisturbed setting, and able to travel to strategic congress conferences

 

#LI-REMOTE

This salary range is an estimate, and the actual salary may vary based on a wide range of factors, including your skills, qualifications, experience and location. This position is eligible for benefits including but not limited to medical, dental, vision, life insurance, disability coverage, flexible paid time off, Spring Health, Carrot Fertility, participation in a 401k with company match, ESPP, and many other additional voluntary benefits. Invitae also offers generous paid leave programs so you can spend time with your new child, recover from your own illness or care for a sick family member.
USA National Pay Range
$137,600$171,900 USD

Please apply even if you don’t meet all of the “What you bring” requirements noted.  It’s rare that someone checks every single item, it’s ok, we encourage you to apply anyways.  

Join us!

At Invitae, we value diversity and provide equal employment opportunities (EEO) to all employees and applicants without regard to race, color, religion, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. We will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the San Francisco Fair Chance Ordinance.

We truly believe a diverse workplace is crucial to our company's success and to better serve our diverse patients. Your input is especially valuable. We’d greatly appreciate it if you can take a quick moment to make your selection(s) below. Submissions will be anonymous.

You can find a detailed explanation of our privacy practices here.

Job ID: 4912918
Employment Type: Other

Perks and Benefits

  • Health and Wellness

    • FSA
    • HSA
    • Health Insurance
    • Dental Insurance
    • Vision Insurance
    • Life Insurance
  • Parental Benefits

    • Non-Birth Parent or Paternity Leave
    • Birth Parent or Maternity Leave
  • Work Flexibility

    • Flexible Work Hours
    • Remote Work Opportunities
  • Office Life and Perks

    • Company Outings
    • Commuter Benefits Program
    • Casual Dress
    • Pet-friendly Office
    • Happy Hours
    • Snacks
    • Some Meals Provided
  • Vacation and Time Off

    • Personal/Sick Days
    • Paid Holidays
    • Unlimited Paid Time Off
  • Financial and Retirement

    • Relocation Assistance
    • Performance Bonus
    • Company Equity
    • 401(K) With Company Matching
  • Professional Development

    • Learning and Development Stipend
    • Promote From Within
    • Access to Online Courses
    • Lunch and Learns
  • Diversity and Inclusion

    • Diversity, Equity, and Inclusion Program

This job is no longer available.

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