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Blueprint Medicines

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1 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Vice President, Medical Affairs (International) Open Medical Affairs Zug CHE Vice President, Medical Affairs Europe Cambridge, MA Requisition number: MEA19-002 At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. Blueprint Medicines is on a journey to becoming a global biopharmaceutical company and is looking for a driven, talented and proven International Medical Affairs leader to help build a significant presence for the company outside the USA. Blueprint Medicines has taken the decision to establish international operations in Switzerland, to prepare for the regulatory submissions and launches of avapritinib, BLU-667 and other assets. The successful applicant will be responsible for building-out the International Medical Affairs function in parallel with Blueprint Medicines’ growth. This is a challenging position offering the opportunity to contribute to the development and success of a truly innovative biopharmaceutical company right from the beginning and to make a real difference to patients’ lives. Developing the International Medical Affairs function in alignment with global strategy requires a hands-on approach. Key aspects of the role include identifying and engaging with KOLs, research and clinical networks in Europe, establishing regional/local advisory boards, developing and driving medical education and communications and playing a pivotal role in any early access programs.  The successful applicant will also be expected to contribute to the design, evaluation and execution of development programs. More broadly, he/she will participate in key decision-making for the company’s Medical Affairs activities through participation in several standing committees and teams. The Precision Medicine Liaison (PML) Senior Director, who, in turn, leads a team of contract PMLs in Europe, will also report into this role. The successful candidate will be driven to thrive in a biotech environment, be comfortable with ambiguity, require conceptual flexibility and possess an entrepreneurial and innovative spirit. The successful candidate will be strategically and operationally strong. This is an outstanding opportunity to have a broad influence on the leadership, development and success of Blueprint Medicines as it builds its presence. Responsibilities: Develop the regional Medical Affairs plan, aligned with global medical and overall corporate strategy.  Implement medical strategies and plans for Blueprint Medicines’ product portfolio in region. Be a highly informed, insightful and active member of the global Medical Affairs team and advocate regional requirements. Remain on the forefront of the relevant science and competitive landscape. Partner with internal stakeholders and functions, while advocating regional imperatives. Identify data/evidence gaps that will impact success and propose solutions to address these. Collaborate with the Pricing & Market Access (P&MA) function to provide medical expertise to help shape P&MA strategies and deliverables (eg/ Dossiers etc.). Collaborate with Commercial organization to ensure timely, accurate and compliant preparation and review of promotional and educational material. Support Commercial teams with disease and product training and advice, and in-field support. Leverage medical knowledge to provide regional perspectives to Business Development activities. Collaborate internally with clinical and regulatory departments to support the planning, execution and management of clinical trial activities. Support studies through site identification, patient identification and clinical trial recruitment initiatives. Contribute to the development of optimized clinical study plans (eg. highlight relevant endpoints, patient populations, etc.) with respect to regional requirements. Work closely with Clinical Development and Operations to ensure appropriate institutions and academic centers have opportunities to participate in Blueprint’s clinical programs. Establish professional relationships with the medical community and PAGs, and exchange scientific knowledge with global and regional opinion leaders to identify current and future business opportunities and emerging medical and health care practices. Represent regional Medical Affairs requirements in the development of Global projects and associated activities including Publication Planning, Advisory Boards, Educational Programs, Conferences. Respond to requests for medical information, as needed. Represent regional requirements in publication and congress plans. Work with internal team to develop key scientific statements on disease, MOA, target product profile, molecular diagnosis, etc. Recommend speaker-programs on Blueprint Medicines’ disease-states, therapeutics and patient care gaps. Represent Blueprint’s brand and present data at advisory boards, clinical investigator meetings, congresses, etc. Contribute to design and implementation of any pre-approval/compassionate access programs. Develop and effectively manage budget and operating plan for regional Medical Affairs. Qualifications: The ideal candidate will bring deep experience in Medical Affairs in the European biopharmaceutical industry, complemented by an understanding of drug development and the pan-European dynamics for market access, launch and lifecycle management. They will have executive presence, self-sufficiency, energy and drive to take this opportunity and run with it, with a collaborative mindset, and honed communication and leadership skills. They will have a level of comfort at working in a high-growth, fast-paced matrix environment, where influencing and negotiating are prerequisites. MD, PharmD or PhD with Oncology experience is required; a minimum of 10 years of medical affairs or clinical research experience within the pharmaceutical industry, CRO health-related consulting company or biomedical/clinical experience within academia (or a combination of aforementioned). Track record of success in building and leading teams and strong managerial experience essential. Previous experience leading MSL teams is an advantage. Track record cultivating a high-performance organization; effective as a mentor and coach; able to attract, develop, motivate and retain key talent.  Ability to think innovatively about medical affairs strategy and anticipate future consequences and trends Well-grounded in drug development with extraordinary leadership competencies and the strategic business perspective needed to bring products forward successfully. Demonstrated ability to lead by example and model collaborative behavior by soliciting opinions, coupled with the ability to make key decisions and be effective in getting the teams behind the decisions. Excellent written and verbal communication and high-level negotiation skills. Ability to interact and communicate openly and effectively with Senior Management, external opinion leaders, regulatory bodies and development team members. Experience developing and executing strong proposals formal presentations to Senior Management and external opinion leaders. Strong analytical skills, especially with regards to understanding and interpreting scientific and clinical research and literature are essential. Demonstrated self-starter and team player with strong interpersonal skills. Adept, nimble and energetic in a fast-paced, dynamic and collaborative environment. Capable of taking a hands-on approach and willing to “roll up one’s sleeves. Experience in cross-functional and cross-cultural markets. Extensive travel is required as part of this position (50%). The candidate should also demonstrate a leadership style that fits within our culture. They must demonstrate the highest integrity and ethical behaviour, mutual respect for our people, a true passion for science and in making a difference in patient's lives. They must be able to work collaboratively within teams, use resources carefully and build a great place to work and grow. All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
2 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM General Manager, DACH Open Chief Business Office DEU At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. The successful candidate will build and lead Blueprint Medicines’ local presence in Germany, Austria & Switzerland (DACH), lead and execute local pricing and market access activities, and develop broader local plans for world-class launches and ongoing success. Reporting to the Senior Vice President & General Manager, International, this is a unique opportunity for a strong German market leader to develop something completely new and play a key role on the broader European Leadership Team.   As Blueprint Medicines is now in the process of building its European organization, this is therefore an exceptional and highly visible opportunity for a dynamic general manager to build a world-class local organization and drive P&L performance. The successful candidate should be a dynamic biopharmaceutical leader, who is able to build something amazing. This person will have proven abilities as a commercial leader, perhaps as a General Manager, a Business Unit Leader or a Sales and Marketing Leader, in the biopharmaceutical industry. S/he will have led successful product launches, driven revenue growth and have a strong reputation for excellent cross-functional collaboration.   Responsibilities: Represent Blueprint Medicines in the DACH region. Uphold high professional standards at all times, with respect to the internal organization and externally. Create and drive a high-performing, dynamic culture by fostering innovation, customer-focus, personal accountability, business acumen and a commitment to success. Ensure adherence to all relevant legal, regulatory and compliance requirements, corporate policies and procedures, and drive this culture in the local organization. Recruit, hire, train and retain top talent. Build and execute launch plans for Blueprint Medicines’ products in DACH, including but not limited to, avapritinib and BLU-667, establishing ambitious revenue growth and profit targets, coupled to prudent cost management. Maximize the potential of this life-changing portfolio. Identify, propose, develop and execute local pricing and market access (P&MA) strategies that are consistent with European P&MA strategy. Establish strong working relationships with external bodies as needed (Payors, Policy makers, Patient Associations, KOLs, etc). Foster an environment of strong cross-functional collaboration at Blueprint Medicines, within the local organization, regionally and globally.  Identify and champion business development opportunities. Qualifications: Undergraduate degree required, MBA and/or post graduate preferred. A broad, multicultural cultural awareness, ideally with some international experience. Excellent written and oral communication skills, including strong formal presentation skills. Ability to manage up, across and down. Strong commercial leadership experience in the biopharmaceutical industry, either as a General/Country Manager, a BU Lead or a Sales and Marketing Lead within DACH markets. A successful track record overseeing product launches, within the Oncology, Haematology or Orphan drug arena. Impressive experience and success in developing and executing market access and reimbursement strategies. A thorough understanding of the market access and reimbursement environment and processes in DACH (esp. AMNOG). An ability and appetite to build relationships rapidly with KOLs and other key external stakeholders. Fluency in both English and German. Capabilities: A high degree of emotional intelligence, displaying candor and integrity at all times. An entrepreneurial and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal. Executive presence. Strong leadership qualities with the ability to attract talent, drive high performance and create a collaborative culture, fostering open communication, constructive conflict and organizational flexibility. Self-sufficiency, energy and drive to take this opportunity and run with it, with exceptional communication and leadership skills, as well as a level of comfort at working in a high-growth, fast-paced matrix environment. Ability to influence across the broader organization. A natural tendency to drive business decisions from a patient-centric mindset. Works collaboratively within teams, use resources carefully and build a great place to work and grow. A leadership style that fits within Blueprint Medicines’ culture, with the highest integrity and ethical behavior, mutual respect for our people. All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
3 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM General Manager, France & Benelux Open Chief Business Office FRA At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. The successful candidate will build and lead Blueprint Medicines’ local presence in France, Belgium, the Netherlands and Luxembourg (France/Benelux), lead and execute local pricing and market access activities, and develop broader local plans for world-class launches and ongoing success. Reporting to the Senior Vice President & General Manager, International, this is a unique opportunity for a strong market leader to develop something completely new and play a key role on the broader European Leadership Team. As Blueprint Medicines is now in the process of building its European organization, this is therefore an exceptional and highly visible opportunity for a dynamic general manager to build a world-class local organization and drive P&L performance. The successful candidate should be a dynamic biopharmaceutical leader, who is able to build something amazing. This person will have proven abilities as a commercial leader, perhaps as a General Manager, a Business Unit Leader or a Sales and Marketing Leader, in the biopharmaceutical industry. S/he will have led successful product launches, driven revenue growth and have a strong reputation for excellent cross-functional collaboration.   Responsibilities: Represent Blueprint Medicines in the France/Benelux region. Uphold high professional standards at all times, with respect to the internal organization and externally. Create and drive a high-performing, dynamic culture by fostering innovation, customer-focus, personal accountability, business acumen and a commitment to success. Ensure adherence to all relevant legal, regulatory and compliance requirements, corporate policies and procedures, and drive this culture in the local organization. Recruit, hire, train and retain top talent. Build and execute launch plans for Blueprint Medicines’ products in France/Benelux, including but not limited to, avapritinib and BLU-667, establishing ambitious revenue growth and profit targets, coupled to prudent cost management. Maximize the potential of this life-changing portfolio. Identify, propose, develop and execute local pricing and market access (P&MA) strategies that are consistent with European P&MA strategy. Establish strong working relationships with external bodies as needed (Payors, Policy makers, Patient Associations, KOLs, etc). Foster an environment of strong cross-functional collaboration at Blueprint Medicines, within the local organization, regionally and globally.  Identify and champion business development opportunities. Qualifications: Undergraduate degree required, MBA and/or post graduate preferred. A broad, multicultural cultural awareness, ideally with some international experience. Excellent written and oral communication skills, including strong formal presentation skills. Ability to manage up, across and down. Strong commercial leadership experience in the biopharmaceutical industry, either as a General/Country Manager, a BU Lead or a Sales and Marketing Lead within France/Benelux territories. A successful track record overseeing product launches, within the Oncology, Haematology or Orphan drug arena. Impressive experience and success in developing and executing market access and reimbursement strategies. A thorough understanding of the market access and reimbursement environment and processes in France/Benelux. An ability and appetite to build relationships rapidly with KOLs and other key external stakeholders. Fluency in both French & English. Fluency in Dutch is an additional advantage. Capabilities: A high degree of emotional intelligence, displaying candor and integrity at all times. An entrepreneurial and innovative mindset. Ability to manage though complexity and ambiguity, while focusing on the end goal. Executive presence. Strong leadership qualities with the ability to attract talent, drive high performance and create a collaborative culture, fostering open communication, constructive conflict and organizational flexibility. Self-sufficiency, energy and drive to take this opportunity and run with it, with exceptional communication and leadership skills, as well as a level of comfort at working in a high-growth, fast-paced matrix environment. Ability to influence across the broader organization. A natural tendency to drive business decisions from a patient-centric mindset. Works collaboratively within teams, use resources carefully and build a great place to work and grow. A leadership style that fits within Blueprint Medicines’ culture, with the highest integrity and ethical behavior, mutual respect for our people. All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
4 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM General Manager, UK/Ireland & Nordics Open Chief Business Office GBR At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. Blueprint Medicines is on a journey to becoming a global biopharmaceutical company and therefore has taken the decision to establish European operations to prepare for the regulatory submission, commercialization and launch of Avapritinib and BLU-667, as well as the company’s R&D pipeline in due course (and any future corporate development initiatives). As such, Blueprint Medicines now wishes to recruit a VP & General Manager UK & Ireland to set up its business in these key markets from scratch. This role will ultimately be responsible for the performance and P&L within the UK & Ireland, with ‘success’ defined by accelerating broad access for patients to the emerging Blueprint Medicines portfolio. Reporting to the Senior Vice-President & General Manager International, this is a unique opportunity to build out the UK & Ireland organization from the beginning and to play a key role, as part of the broader EU Leadership Team (and overall global commercial team), in the development of Blueprint Medicines in Europe. The successful candidate for the position of VP & General Manager UK & Ireland will be a recognized biopharmaceutical leader who is naturally autonomous and a self-starter. In addition to the industry and functional experience in general management, the successful individual should bring a demonstrable knowledge of public/governmental and medical affairs, special access/named patient programs as well as market access and pricing/reimbursement more broadly within the UK & Irish markets.   Personal characteristics will be absolutely crucial, as the successful individual needs to have the self-sufficiency, energy and drive to take this opportunity and run with it, with exceptional communication and leadership skills, as well as a level of comfort at working in a high-growth, fast-paced matrix environment, where influencing and negotiating across an organization are a prerequisite. The candidate should also demonstrate a leadership style that fits within Blueprint Medicines’ culture. The successful candidate will demonstrate the highest integrity and ethical behavior, mutual respect for people, a true passion for science and in making a difference in patient's lives, works collaboratively within teams, uses resources carefully and can build a great place to work and grow. Responsibilities: Build and execute the strategic launch plan for Avapritinib and BLU-667 in the UK & Ireland. Recruit, hire, and ensure training for country specific staff who will execute the commercial plan in the UK & Ireland. Aggressively drive the development Blueprint Medicines’ business, establishing growth and profit expectation and ensuring effective financial planning.   Establish market sales and resource forecasts, and also initiate relevant market research projects to support the strategic brand planning process. Identify, develop, propose and execute local reimbursement strategies including adaptation and communication of the value story to key local stakeholders. Maximize the commercial potential of Blueprint Medicines’ assets through the development and implementation of strategic marketing plans in collaboration with Regional/ Global Marketing and Medical Affairs. Establish strong and optimal relationships with external bodies (Payors, Patient Associations, and KOLs) as relevant. Foster an environment of strong collaboration across the local, regional and global organization, balancing the needs of Blueprint Medicines in the UK & Ireland with those of the broader corporate objectives.  Serve as point person responsible for managing and optimizing local partnerships and provide commercial input for business development opportunities. Ensure that all business activities are in line with company policies, procedures and local guidelines. Facilitate market learning and knowledge sharing to accelerate the commercialization of Avapritinib and BLU-667 (as well as future products) throughout EMEA. Drive a high-performance culture by fostering innovation, customer focus, personal accountability and commitment for results. Qualifications: Demonstrable and meaningful commercial leadership experience in the UK & Ireland biopharmaceutical industry, either as a General Manager/Country Manager currently or a BU Director. Successful track record of overseeing product launches in the UK & Ireland, preferably with more than one product within the Oncology/Haematology arena Demonstrable involvement in access and reimbursement strategies and execution, with the ability to shape and articulate the value story of speciality therapeutics. Possess a strong and robust personal and professional network with the likes of NICE, SMC, AWSMG, whilst being adept at building new relationships rapidly with KOLs and other stakeholders such as industry associations. Innate ‘market-making’ capabilities. Knowledge of the technical development of commercially successful biopharmaceutical products. A natural self-starter, hands-on with the ability to shape and build a business. The ability to drive business decisions from an innately patient-centered mindset, and with the ambition and commitment to make a major impact on human health. Strong leadership qualities with the ability to attract talent and create a culture of collaboration and teamwork that fosters open communication, constructive conflict and organizational flexibility. Broad cultural orientation, ideally with some experience of working outside the UK & Ireland in an international context. Excellent written and oral communication skills, including strong formal presentation skills. Entrepreneurial and innovative of spirit. Learning agile and ‘scalable’ to take on increasing responsibility as Blueprint Medicines grows both within and outside the UK, Ireland & Nordics. High degree of emotional intelligence, displaying candor and integrity at all times. Ability to manage complexity, ambiguity and paradoxes.    Fluent in English; other languages advantageous. Undergraduate degree required, MBA and/or post graduate preferred. All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
5 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Associate Director, Intellectual Property Open Legal Cambridge MA USA Associate Director, Intellectual Property Cambridge, MA   At Blueprint Medicines, as our name indicates, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy.   Job Summary: Blueprint Medicines seeks an exceptional candidate for an Associate Director of Intellectual Property.  The successful candidate will possess significant experience in the development and protection of intellectual property of small molecule pharmaceutical assets. This position reports to the Director, Intellectual Property. Responsibilities: Works in collaboration with the scientific and clinical staff to build strong patent portfolios around key assets to ensure long-term competitive advantage.  Responsibilities include to identify and evaluate new inventions, conduct prior art searches, manage new and existing patent portfolios, respond to administrative challenges instituted by third parties, including oppositions and inter partes reviews, and monitor competitive intellectual property Partners with program teams to manage all aspects of intellectual property for programs, including patents, trademarks, copyrights, and trade secrets world-wide Supervises and directs outside patent counsel in patent preparation and prosecution and assessment of infringement claims Designs and analyzes freedom-to-operate searches, evaluates issued patents, prepares or obtains analysis, and ensures that management is informed on aspects of intellectual property rights owned by other entities Works with internal clients and in-house counsel on IP aspects of contracts and agreements, including IP-related business development licensing opportunities and transactional work Reviews intellectual property aspects of technical manuscripts, posters, and other materials intended for publication When appropriate, enforces the company's intellectual property rights through investigation of competitors' products and supports negotiation of favorable intellectual property licenses and litigation Qualifications: Advanced degree in organic chemistry, Ph.D. preferred Must be registered to practice before the U.S. Patent and Trademark Office J.D. and bar admission in at least one state At least 3 years of law firm experience with emphasis on small molecule patent prosecution 2-3 years of in-house pharmaceutical company experience, including management of a complex IP portfolio and experience managing high volume intellectual property workflow Knowledge of small molecule pharmaceutical patent strategy including 505(b)(1), 505(b)(2) and ANDA related proceedings strongly preferred Capabilities: The ability to work both in a strategic high-level project mode, as well as tactically, including the capability and willingness to “roll up one’s sleeves” regularly Understands the interrelationship between the legal, scientific and business aspects of intellectual property and the use of IP to further the company’s business goals Demonstrates business partner orientation and ability to recognize and to respond quickly, clearly and pragmatically to urgent situations Excellent interpersonal skills that are demonstrated by being articulate, direct and forthright, and serving as a collaborative and decisive team member and a strategic thinker with a broad perspective Ability to manage and prioritize multiple matters simultaneously and to respond to rapidly shifting priorities in ambiguous or challenging situations Comfortable and adept at balancing risk and opportunity At home in a results-driven, highly accountable environment where you can make a clear impact A team player, who listens effectively and invites response and discussion A collaborator who communicates in an open, clear, complete, timely and consistent manner All applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status. All applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability or protected veteran status.  WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
6 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Associate Director, Total Rewards Open Human Resources Cambridge MA USA Associate Director, Total Rewards Cambridge, MA Requisition Number: HR910 At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. We have an exciting opportunity for an experienced, hands-on Total Rewards professional with a desire to positively contribute to a rapidly growing, mission-driven global biotech.  This person will lead efforts in the design, execution and communication of our total rewards programs ensuring they are competitive, sustainable, scalable and have a positive impact on the overall performance of Blueprint.  Responsibilities of this position will have a strong emphasis on benefit programs. This role also has a unique opportunity to be on the ground floor of broader HR initiatives as we embark on the next chapter of the Blueprint Medicines story. Responsibilities: Design, implement and drive competitive total rewards programs, including, but not limited to benefits and perks that attract and retain our talent and align with market trends Oversee the management of our benefits and wellness vendor relationships, monthly billing and budget management, benefits contracts, and bid negotiation Be a visible, consultative total rewards advisor who ensures programs are fully integrated, understood and valued by employees and are aligned with other talent management initiatives. Analyze the market competitiveness and cost-effectiveness of our benefits and compensation programs and plans to ensure they optimize our ability to attract and retain top talent Leverage technology to develop the technical systems, automated business processes and workflows that support total rewards program delivery (benefits, perks, recognition and compensation). Provide insightful data to guide decision making and offers proactive solutions Ensure compliance with all governmental regulations related to benefit and compensation programs Qualifications: Bachelor’s degree in Business Administration, Finance, Human Resource Administration A minimum of 10 years designing and implementing Total Rewards Programs; minimum 5 years experience in the biotechnology industry Experience with international compensation and benefits preferred Current knowledge of related government rules and regulations, including, but not limited to ERISA, FLSA, FMLA, ADA, ADAA, COBRA, OSHA, HIPAA, Workers’ Compensation, and other applicable Labor and/or Tax laws and regulations; fulfills compliance and reporting requirements Knowledge and experience across the spectrum of broad-based total rewards and in-depth understanding of benefits design and administration In-depth knowledge of the benefits marketplace including differences between insurers, marketplace trends, benchmarking and changes in the legislative framework affecting benefits Capabilities: A progressive approach to total rewards strategy, design and implementation Strong sense of urgency that enables a proactive, consultative approach to seize opportunity and solve problems. Strong systems aptitude and HRIS experience Excellent computer skills, including MS Office Enthusiastic team player with strong service orientation Excellent verbal, written and interpersonal communication skills Strong organizational skills with the ability to prioritize and multi-task Ability to develop trust and confidence among all levels within the company Adaptable and flexible to changes in work load and priorities Ability to grasp and implement new concepts in a timely fashion leveraging excellent time/project management skills. At home in a results-driven, highly accountable environment where you can make a clear impact. A team player, who listens effectively and invites response and discussion. A collaborator who communicates in an open, clear, complete, timely and consistent manner. All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
7 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Associate/Medical Director, Drug Safety and Pharmacovigilance Open Pharmacovigilance Cambridge MA USA Associate/Medical Director, Drug Safety and Pharmacovigilance Cambridge, MA Job Req: PV19-003   At Blueprint Medicines, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy.   Job Summary: Reporting to the VP, Drug Safety and Pharmacovigilance, the Medical Director is responsible for the medical assessment of Individual Case Safety Reports (ICSRs) and other drug safety information. The individual will be responsible for assessing and interpreting safety data from multiple sources, including clinical trials, spontaneous and solicited reports, aggregate, and literature reports. This physician is expected to provide interpretation and summaries of drug safety information and provide input in the generation of safety reports (e.g., DSURs, PSUR and clinical safety assessments). The individual will be an integral part of a group of safety professionals within Blueprint Medicines and will closely collaborate with safety teams in Contract Research Organizations (CROs) and partners. He/she will need to maintain medical knowledge as required by the role, strong and current knowledge of drug safety and pharmacovigilance regulations, pharmacovigilance practices, safety surveillance and risk-management practices.   Responsibilities: Provide medical expertise in the assessment of ICSRs and aggregate drug safety reports Review, analyze, and compile safety data, and present the results Contribute to the generation of aggregate safety reports including development safety update reports, periodic benefit risk evaluation reports, and provide medical input in review of new or existing safety documents to ensure compliance with relevant regulatory requirements, such as protocols, safety summaries and regulatory reports Support of the internal PV Operations function Contribute to ongoing safety surveillance and signal detection efforts Contribute to signaling and safety surveillance process, including the identification of safety observations, emergent safety concerns and new safety signals, ensure prompt assessment and communication of confirmed safety signals Serve as a medical resource for the generation and review of clinical trial protocols, informed consent forms (ICFs) and investigator brochures (IBs) Provide medical safety input into the development of Reference Safety Information Contribute to creation or and updates to Risk Management Plans (RMPs) and/or Risk Evaluation and Mitigation Strategies (REMS) and the maintenance of these documents Provide medical safety and Pharmacovigilance expertise in-house and by consultation with outside vendors for all development programs Contribute to the development of Standard Operating Procedures, Working Instructions and other guidance documents Contribute to safety and pharmacovigilance training programs Provide safety training at investigator meetings Present safety data and results Collaborate with Regulatory Affairs to ensure appropriate reporting of pharmacovigilance and drug safety information to regulatory agencies and prescriber community Collaborate with Medical Directors and Clinical Research Scientists, and vendor clinical staff who provide medical monitoring support for ongoing clinical trials Develop relationships with and capture drug safety information from key groups, including partner companies, physicians, nurses and patient advocacy groups Serve as a subject matter expert for vendors providing drug safety and pharmacovigilance services Qualifications: 2+ years’ experience in Drug Safety / Pharmacovigilance in a pharmaceutical or biotech company, CRO or regulatory agency Medical Degree (MD) from recognized medical school with medical practice experience Good working knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines Demonstrated experience with medical drug safety assessments, drug safety surveillance and monitoring activities Proficiency with medical review of ICSRs, including expectedness assessments, causality assessments, narrative review and generation, generation of Analysis of Similar Event and company comment statements, including benefit-risk assessment. Experience with safety data collection and interpretation originating from clinical trials and other sources (such as literature, solicited and post-marketing environment) Experience with the medical review and preparation of aggregate reports (DSUR, PSUR/PBRER, PADER) Experience with preparation of responses to Regulatory Authorities, preferred experience with IND/NDA submissions and negotiations with Regulatory Authorities as part of marketing approval Experience with the development and updates to Reference Safety Information, including IB, Company Core Data Sheet (CCDS) and local labels Ability to build relationships, collaborate and influence across disciplines within Blueprint Medicines and with outside stakeholders Experience with MedDRA coding, Points to Consider, AoSE, and SMQs Excellent verbal, written and presentation skills   All applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
8 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Senior Director, Translational Medicine Open Translational Medicine Cambridge MA USA At Blueprint Medicines, as our name indicates, we are creating a blueprint for the future of healthcare. We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically-defined cancers, rare diseases and cancer immunotherapy.  Blueprint Medicines is looking for a highly motivated, creative and collaborative translational medicine leader with deep scientific expertise, leadership experience and the passion for bringing benefit to patients using precision medicine. This is a great opportunity to join a high-growth company that is focused on identifying the right patient population for our innovative, experimental medicines with even greater precision. As a member of our translational medicine team, you will be a vital part of shaping our translational strategy and vision. The candidate is expected to have a cutting-edge understanding of latest technologies and trends in Oncology, as well as Immuno-Oncology, therapeutic development. Responsibilities: Develop and coordinate biomarker, patient selection and companion diagnostic strategies for projects across Blueprint’s growing oncology portfolio Lead the development, outsourcing and validation of clinically relevant biomarker assays (e.g., pharmacodynamic, predictive, prognostic and safety biomarkers) Lead the development and implementation of companion diagnostic strategies, including co-development with in vitro diagnostic partners Support global regulatory strategy and contribute to the generation of investigator brochures, IND applications, clinical protocols and other regulatory documents as appropriate Provide deep domain area expertise to discovery and development project teams and further enhance Blueprint’s scientific reputation through high impact publications and presentations Function as a scientific and business thought-leader inside and outside of the company and a key link to external community Qualifications PhD in molecular oncology, molecular/cell biology or immunology with relevant post-doctoral training 8+ years of pharmaceutical or biotechnology industry experience in Oncology/Cancer Immunotherapy with expertise in oncology biomarker and companion diagnostic development Ability to drive and influence projects from discovery through early clinical development with a focus on the identification of biomarkers of response and/or resistance to therapy In depth experience in the discovery, validation and clinical implementation of innovative biomarkers and companion diagnostics Excellent leadership, organizational, written and presentation skills working in a matrixed team environment Capabilities: Demonstrated application of expertise to discovery research through early clinical development in the area of oncology and/or immuno-oncology Familiarity with engaging and managing external efforts with contract research organizations and academic collaborators Familiarity with data management and visualization tools and collaborating with computational biology to analyze complex genomic data sets emerging from clinical trials At home in a results-driven, highly accountable environment where you can make a clear impact A team player and mentor, who listens effectively, invites response and discussion and promotes creative problem solving Ability to embrace Blueprint’s core values: Patients First, Thoughtfulness, Trust, Optimism and Urgency All applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
9 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Senior Director, Head of Global Patient Affairs Open Corporate Affairs Cambridge MA USA At Blueprint Medicines, as our name indicates, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicine to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy. We are seeking an exceptional candidate to develop and lead a patient advocacy team at Blueprint Medicines within the corporate affairs functions. Reporting to the Vice President of Corporate Affairs and managing a team of advocacy professionals, the Head of Global Patient Advocacy will oversee partnership and engagement strategy with global patient advocacy groups across the company’s portfolio, patient and carer insight gathering and analysis to inform clinical and program strategy, patient preferences and data that assist in value demonstration, and patient education and engagement programs. In addition, the candidate will help to establish Blueprint Medicines’ leadership within the broader oncology and rare disease patient advocacy communities, and champion the patient perspective within the company. The right candidate will have strong leadership skills, be an excellent communicator with an ability to develop meaningful relationships, a strategic thinker that can bridge the complexities of patient care and drug development and access, a seasoned collaborator who can successfully lead and influence external and internal stakeholders, and a highly motivated self-starter who is comfortable innovating in an entrepreneurial and fast-paced start-up company environment. Responsibilities: As a functional leader, help define Blueprint Medicines’ vision and mission for patient advocacy, and build strategy that reflects the company’s commitment to patient, carer, and advocate engagement Build an infrastructure that ensures advocacy strategy and programs advances the interests it shares with advocates along the development and commercialization continuum Champion the patient perspective and deliver strategic insights to senior executive, clinical development/operations, medical affairs, HEOR, commercial leaders, as well as program teams, to optimize corporate and program strategy Foster a patient-centric culture driven by our core value “patients first”, directly connecting employees to the patient and carer experience through distinct and innovative corporate programs and activities Oversee development and implementation of strategic plans for engaging [global] patient communities across Blueprint Medicines’ portfolio, with an emphasis on clinical-stage programs Oversee engagement at patient meetings across the portfolio, ensuring activities demonstrate Blueprint Medicines’ commitment to disease communities and drive strategic program goals Be the key relationship manager for [global] patient advocacy groups; oversee regular communications by the advocacy team and ensure other cross-functional alignment; assess and mitigate potential risks Identify, initiate and oversee strategic patient advocacy programs and partnerships related to disease awareness and education, diagnosis, access to appropriate care, adherence, and policy Drive clinical trial design, awareness and patient identification initiatives across the portfolio to support rapid trial enrollment and execution Lead or contribute to the development of patient-facing educational materials across the portfolio Partner effectively with medical affairs and clinical to ensure patient inquiries about our programs, including clinical trials and pre-approval drug access, are rapidly and consistently addressed with compliant information Partner effectively with legal, regulatory, clinical, medical affairs and finance to optimize a strategic and compliant sponsorship, grants and charitable contribution review process Manage a team of two advocacy professionals, including their professional development, and contribute to corporate affairs workforce management and planning Create and ensure adherence to legal and compliance frameworks that ensure the company’s relationships with advocacy stakeholders are respectful and appropriate  Routinely interact and build trusted relationships with executive leadership, EU/international leadership, commercial, medical affairs, clinical, research, legal, and regulatory Oversee the advocacy budget, identify and supervise management of external strategic partners Reinforce Blueprint’s leadership role within industry via external involvement; board membership, committee, speaking engagements Qualifications: Bachelor’s degree required; advanced degree preferred (e.g., MS, RN, PhD, or MD) Minimum 10 years of relevant patient advocacy, communications or consumer marketing experience in the biopharmaceutical industry; overall 15+ years of relevant industry or non-profit experience Proven understanding of the needs of individuals living with cancer and rare diseases as well as pressing public health issues, including patients and care providers Knowledge of the biopharmaceutical industry, with an understanding of regulatory bodies that impact communications and reimbursement Understanding of guidelines and best practices for developing and executing patient outreach programs and patient events in the US and Europe High degree of professionalism, maturity, executive presence, business understanding and confidentiality Strong written and verbal communication skills as well as strong interpersonal skills, with impeccable attention to detail Strong leadership skills with a proven ability to collaborate effectively with internal and external stakeholders at all levels and influence decision-making without authority Highly motivated individual with the flexibility and creativity to excel in a rapidly growing and changing environment; confidence and organizational skills to independently work on multiple tasks Must be willing and able to travel (approximately 30%) and regularly meet with patient advocacy organizations in the U.S. and internationally All applicants will receive consideration for employment without regard to race, color, age, religion, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology
10 nasdaq:bpmc blueprintmedicine.applytojob.com blueprintmedicine.applytojob.com Apr 4th, 2019 12:00AM Clinical Study Manager Open Clinical Operations Cambridge MA USA Clinical Study Manager Cambridge, MA Job Req: CLO19-002   At Blueprint Medicines, as our name indicates, we are creating a blueprint for the future of healthcare.  We are a leading company in the personalized medicine revolution by focusing on delivering new medicines that are targeted to the genetic driver of disease.  We do this by leveraging our one-of-a-kind drug discovery platform to discover, develop and work to bring highly-selective kinase inhibitors to patients globally.  This prolific scientific platform has enabled Blueprint Medicines to build a pipeline of novel therapies that span three distinct areas of medicine; genomically defined cancers, rare diseases and cancer immunotherapy.   Job Summary: This position reports into the Associate Director of Clinical Operations (or above).   The right candidate will possess an understanding of Clinical Operations for successful execution of multiple clinical trials primarily in oncology and hematology indications in various phases of development.   Responsibilities: Responsibilities of this position involve the day to day management and oversight of clinical trials in collaboration with a dynamic Clinical Development team.  Specific Responsibilities include: Independent management of the operational aspects of Blueprint Medicines’ clinical trials, including vendors such as CROs, central labs, biomarker and specialty laboratories, and clinical trial sites. Identification and qualification of clinical trial sites and investigators alongside CRO including management of key relationships.   Participation in final decisions for site selection with Blueprint Medicines’ team.   Participation in the day to day supervision of clinical trial execution, with a focus on site start up, patient enrollment, monitoring, compliance, and data flow metrics from the clinical sites, CROs and central labs Management of clinical study budgets and execution timelines. Leads internal team meetings for study management. Facilitation of investigator meetings, kick-off meetings, monitoring training, and various CRO (or other vendor) meetings. Participation in the development of clinical trial protocols, amendments, CRFs, IRB/Ethics applications, and recruitment materials. Attendance at site visits to ensure oversight of CRO monitors and effective collaboration with Investigators and site staff. Review study reports and metrics to ensure timely collection of clinical data, samples, and lab results. Collaboration on SOP development and promotion of standardized clinical business tools. Development and review of specific study documents e.g. informed consent forms, study guidelines, operations manuals, training materials. Development of action plans to address protocol compliance, safety, data and administrative issues with investigational sites and CROs. Participation in the preparation of presentations of trial data for internal and external parties (management review, scientific meetings, and advisory boards).   Qualifications: Minimum Education Required: Bachelor’s degree in a scientific discipline required. Advanced scientific degree is preferred. The candidate should ideally have 4-6+ years in trial management with a sponsor company managing various phase clinical trials.  Experience in various phases of clinical trials and various therapeutic areas, including oncology, would be helpful. Experience in CRO, vendor and laboratory oversight is required. Motivated self-starter who is capable of flourishing in a fast-paced small company environment. Creative problem solver with excellent communication and public speaking skills. Strong interpersonal and organizational skills are needed, with a high degree of attention to detail.  Ability to interact well with individuals at all team levels (e.g., Clinical scientist, Project leader, Physician, etc.). Ability to travel for up to 30% of time, both domestic and international, may be needed. Detailed knowledge of GCP and current US FDA regulations, and knowledge of other relevant global regulatory requirements a plus.   All applicants will receive consideration for employment without regard to race, age, color, religion, age, sex, national origin, disability or protected veteran status. WHO WE ARE: Blueprint Medicines’ mission is to dramatically improve the lives of patients with genomically defined diseases. Our singular focus is to use our deep understanding of the genetic blueprint of cancer and other diseases driven by the abnormal activation of kinases to craft highly selective medicines aimed at eradicating these diseases. We don’t think in small steps. We think in giant leaps. We are driven by the pursuit of new ideas, new innovations, and new ways of thinking. We know that what each and every one of us does matters and that our success depends on our ability to work together. We believe we are at our best as a company when our employees are thriving and foster a culture that provides opportunities to grow and develop professionally, while also having fun. Apr 4th, 2019 12:17AM Apr 4th, 2019 12:17AM Health Care Pharmaceuticals & Biotechnology

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