Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
Responsibilities will include, but are not limited to, the following:
Medical Lead for Franchise specific priorities within G3M teams Support the VP GMADL in early pipeline disease strategy and compound development aspects Lead Medical Affairs sponsored studies as applicable, ie planning & execution within appropriate standards for compliance, quality, timeliness, and budget Oversee Medical activities (tactical) implementation of global Medical compounds of the brand/disease plans Partner closely with regions on key Medical Education opportunities, track performance to goals/budget and Key Data Generation opportunities Identify and oversee projects of real-world-data collection and registries Partner with Scientific Communications on publication strategy, gap analysis, and key messages Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy and tactics with appropriate use of resources and performance to goals Partner very closely with commercial counterparts, CRD, translational as well as regulatory, project leadership and market access Assist Global Disease Lead as necessary for various activities of Global Disease Strategy Team Represent GMA on behalf of the Disease Lead as a therapeutic area expert in both internal and external venues including the DST, clinical sub-teams, and advisory boards / steering committees Lead/support various Medical Affairs cross-functional working groups and collaborate with other GMA disease team members High quality scientific/clinical input and review of: Disease strategy/plans, abstracts, posters, slides, manuscripts in disease area, educational materials in disease area including slides, webcasts, etc., LOIs/ IIT protocols in disease area, steering committee and advisory board meeting objectives, materials, CTB, booth panels, Med info letters, CDPs, Commercial Brand plans, Integrated Disease Plans, ORQs in disease area, Scientific educational grant requests and patient advocacy grant requests Represent Celgene at professional meetings, congresses, and local symposia Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations Be a key partner to external stakeholders, as a scientific & strategic expert: key opinion leaders, cooperative study groups, Investigators, contribute and conduct global steering committees, scientific & strategic global advisory Boards, partner with advocacy groups
*LI-POSTCelgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.
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Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.