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Associate Director, Scientific Communications & Training

Blueprint Medicines
United States, Massachusetts, Cambridge
45 Sidney Street (Show on map)
Aug 28, 2025

How will your role help us transform hope into reality?

The Associate Director, Global Scientific Communications and Training is a vital member of the Global Medical Affairs team who will create and lead the function/team of Scientific Communications reporting into the Director of Global Medical Information, Scientific Communications and Training. You will lead the development and execution of scientific communications strategies and training plans for all Blueprint Medicines therapeutic areas, world-wide. This highly visible role will collaborate cross-functionally with Project teams, Clinical Development, and the broader Medical Affairs team, in the oversight of medical activities for a portfolio of products in Oncology, Hematology, Immunology and Allergy, and Rare diseases.

You will lead the development and execution of comprehensive training strategies across Blueprint Medicines' therapeutic areas, including Oncology, Hematology, Immunology, and Rare Diseases. This role is pivotal in equipping internal and external-facing teams with the scientific fluency and tools needed to engage confidently in discussions and deliver impactful communications.

You will assure that medical and scientific results from BPMC studies are communicated in an accurate, timely, compliant, and compelling manner. This position plays a major role in supporting development of global scientific content for use externally. You are responsible for contributing to the cross-functional short- and long-term strategic development and tactical execution of medical and scientific materials, MSL materials, and digital Medical communications.

You will also be responsible for evaluating, refining and developing new processes where needed and bringing your experience to bear on the development of policies and procedures as Blueprint prepares for the next stage of its growth.

What will you do?



  • Develop and implement robust training curricula focused on disease state awareness, product knowledge, and treatment landscape.
  • Lead onboarding and sustainment training for internal teams, including new hires and field medical personnel.
  • Work closely with Clinical Development, Compliance and Commercial teams to ensure training aligns with broader organizational goals
  • Contributes to the development of the global scientific communications strategy (exclusive of publications) and dissemination of data externally (inclusive of HEOR/RWE data)
  • Generates and review scientific content for many scientific communications-related activities such as global slide decks, digital assets, medical Q&A, and congress booth resources for accuracy
  • Brings insights into the development of innovative tools for internal and external communications
  • Leads the development of scientific communication plans for BPMC assets and leverages publication/data dissemination plan for the creation of simultaneous and aligned enduring materials and educational activities
  • Develop and manage Medical Affairs communication activities at scientific congresses; serve as a key advisor on congress/convention best practices and long-term strategy
  • Ensures awareness of BPMC specific assets internally by circulating and presenting to field medical
  • Ensures clinical trial awareness materials available to MSLs to supplement trial recruitment activities
  • Manage vendors and budgets to execute on agreed-upon tactics and projects often executing on multiple projects simultaneously
  • For all deliverables, collaborate with congresses, medical experts, and will liaise with cross-functional internal team including clinical development, medical, and marketing
  • Maintain a thorough understanding of disease biology, scientific data, and competitive data in order to develop scientifically rigorous and high-quality products and programs



What minimum qualifications do we require?



  • Advanced Clinical/Science degree or professional credentials a plus (MD/DO, PhD, PharmD, PA, NP)
  • A minimum of 5 years of experience in the biotech or pharmaceutical industry focused in Medical Affairs, with experience working with cross-functional in-house and field-based teams
  • Oncology/Hematology/Rare Disease -specific experience required
  • Ability to travel globally as required (15%)



What additional qualifications will make you a stronger candidate?



  • Prior Scientific Communication experience in industry preferred. Will consider agency experience.
  • Strong organizational skills and business planning, including development of a budget and adherence to targets
  • Excellent verbal and written communication skills
  • Attention to detail and strong project management
  • Creative problem-solving skills
  • Manage and adhere to Blueprint medicines policies, ensuring compliance with corporate rules and government regulations
  • Ability to interact and communicate openly and effectively with Senior Management, and commercial and development team members
  • Strong analytical skills, especially with regard to understanding and interpreting scientific and clinical research and literature are essential
  • Adept, flexible, energetic and comfortable in a fast-paced, dynamic and collaborative environment
  • Capable of taking a hands-on approach and willing to "roll up one's sleeves."
  • Commitment to our 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?

Equal Employment Opportunity

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 TotalRewards@blueprintmedicines.com. 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 theU.S.andEurope. 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, visitwww.BlueprintMedicines.comand follow us onX(formerly Twitter; @BlueprintMeds) andLinkedIn.

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