Precision Medicine Executive, Northeast

Location: Boston MA

How will your role help us transform hope into reality

The Precision Medicine Executive (PME) Region will play a meaningful role setting the foundation for commercial success as we deliver through multiple product launches and indication expansions for patients with solid tumors and a rare hematologic disorder. The primary focus will be to improve the diagnosis of systemic mastocytosis to support the commercial success of AYVAKIT. You will be responsible for driving adoption and utilization of quality diagnostic testing in key accounts to identify patients who may be candidates for Blueprint Medicines portfolio of precision therapies in oncology and rare diseases with a focus on systemic mastocytosis . You will report to the Director Precision Medicine Executive Field Leader and be a key member of an efficient effective and highly collaborative field team regionally aligned with field sales.

What will you do

• Be responsible for cultivating stakeholder relationships and developing account-specific plans to facilitate use of high quality biomarker/genomic testing to ensure optimal diagnosis
• Demonstrate knowledge of access to and the ability to build and manage relationships with all key stakeholders in targeted accounts (Pathologist Executive Leadership Lab personnel etc.)
• Apply strong technical acumen to effectively educate on diagnostic testing and disease state to key stakeholders (including broader care team and treating clinicians) and how it fits in the treatment paradigm in SM.
• Deliver educational materials and programs partnering with marketing sales and medical affairs appropriately
• Proactively identify and communicate customer issues educational opportunities and market developments with regional partners and broader Precision Medicine team
• Serve as a diagnostics subject matter expert for the region
• Develop business plans for each target account aligned to strategic imperatives
• Represent Blueprint Medicines at congresses and medical meetings including pathology meetings
• Form relationships with diagnostic laboratories and identify partnership opportunities
• Travel within the US on a regular basis which may include overnight and weekend travel
• Align with regulatory guidelines public policies/guidelines and corporate policies and procedures

What minimum qualifications do we require

• BA/BS degree OR equivalent work experience required
• 5 years experience in biotech pharma or diagnostic laboratory setting
• Ability to travel within the US on a regular basis including overnight and weekend travel
• Candidate must reside in or near Boston MA

What additional qualifications will make you a stronger candidate

• MBA advanced degree in life sciences medical or pharmacy degree preferred
• Strong technical background in pathology molecular biology and/or diagnostics applicable to hematology oncology or rare diseases
• Demonstrated success across multiple drug launches in applicable specialty markets
• Understanding of diagnostics market considerations including regulatory reimbursement and policy as well as familiarity with patient provider and payer perspectives on diagnostic testing
• Strong oral and written communication skills
• Robust analytical and problem-solving skills ability to identify and action on creative solutions
• Ability to establish credibility connect the dots and align multiple stakeholders to pioneer the adoption of new products methods and technologies
• A teammate able to collaborate effectively with a broad range of partners influence without authority gain consensus and act independently in a fast-paced entrepreneurial environment
• Flexibility and the ability to plan and nimbly adapt to changing conditions
• Motivated by patient focus urgency and personal dedication to high performance results and compliance
• Possesses high integrity and exceptional work ethic
• Commitment to Blueprint Medicines Core Values: Patients First Thoughtfulness Urgency Trust Optimism

Why Blueprint

At Blueprint Medicines we achieve impactful results because of our global crew of compassionate innovators the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights which drives our success.

This is the place where the extraordinary becomes reality and you could be part of it.

Patients are waiting. Are you ready to make the leap

Equity Diversity Inclusion and Affirmative Action

At Blueprint Medicines wefoster an environment of fair treatment and full participationforall of our employees as we navigate complex challenges in pursuing our mission to improve the lives of patients. We celebrate our unique differences and varied career and life experiences so that we can sustain our diverse culture and ensure everyone feels accepted. We arecommitted to non-discrimination equal employment opportunity as well as an inclusive recruitment process. We consider all qualified applicants based on merit and without regard to race color sex gender identity sexual orientation age religion national origin ancestry ethnicity disability veteran status genetic information or any other characteristic protected under applicable federal or state law.

We will make reasonable accommodations absent undue hardship for qualified individuals with known disabilities. If you are an individual with a disability in need of an accommodation with the application or recruiting process please reach out to We are also an E-Verify Employer. For more information please see ourEEOPolicy Statement theE-Verify Participation Poster theRight to Work Poster and theEEOKnow Your Rights Poster.

Blueprint Medicines a Sanofi company is a global biopharmaceutical company that invents life-changing medicines. We seek to improve and extend patients lives by solving important medical problems with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success with two approved medicines including AYVAKIT/AYVAKYT (avapritinib) which we are bringing to patients with SM in . Leveraging our established research development and commercial capability and infrastructure we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information visit follow us onX(formerly Twitter; @BlueprintMeds) andLinkedIn.

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