Bristol Myers Squibb Senior Scientific Advisor IO in BUDAPEST, Hungary

Senior Scientific Advisor

Main responsibilities: 1.Collect and communicate medical insights
  • profiling the medical landscape in the focused countries within the Disease Area and continuously update this knowledge, including knowledge and expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities

  • Contribute to the development of Brand Plans and Brand Strategies by communicating medical insight and knowledge about the product or disease area, in particular with reference to patients needs and treatment trends

  • Participate in the development of the Local Medical Plan, work with distributor partner to deliver Local Medical Plan, contribute to the overall Commercial Plan by leveraging medical insight and knowledge of recent scientific publications about the product or disease area

  1. Scientific exchange with Thought Leaders
  • Develop and maintain TL engagement plan in the focused countries

  • Proactively or reactively interact with healthcare providers, through face-to-face meetings, webconferences, teleconferences, e-mail, etc.

  • Contribute to involvement of Thought Leaders in local and/or GDO driven studies, CUP/EAPs and other scientific activities

  • Identify the need for and execute local Advisory Boards

  1. Provide medical services to external customers / partners
  • Present information to HCPs ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives

  • Propose scientifically meaningful medical programs such as Continuous Medical Educational Programs and Symposia and ensure flawless execution of such activities

  • Identify potential speakers for BMS educational programs and ensure that these speakers receive all necessary product and disease state training.

  • Provide scientific information to and collaborate with business/distributor partners’ relevant functions

    4. Medical support for internal stakeholders
  • Contribute to the initial and ongoing medical/scientific disease area and product-specific training of internal BMS stakeholders (specifically to Commercial, Regulatory, Pharmacovigilance, Legal Counsel and Market Access), Investigational Site staff, Site Managers and Monitors in BMS products

  • Contribute to, supervise and coordinate the development of the medical / scientific sections of pricing and reimbursement files

  • Contribute to the development and review of non- promotional material (consistent with the Non-Promotional Review SOP) and also participates in the review process of Risk Minimisation Materials / ARMA materials

  • Endorse and implement a culture of compliance

  • Convey a clear message on legal and ethical standards to Expert Physicians and Investigators

  • Medical doctor (physician), PharmD or PhD, with experience in a specific Disease Area or with a broad medical background or Science graduate with substantial and relevant pharmaceutical experience

  • Excellent English language skills, both written and spoken

  • Experience with working in a scientific and /or clinical research environment

  • Motivated and quick learner, able to effectively communicate and present scientific and/or clinical data to research or healthcare professionals and to train others

  • Able to translate scientific or clinical data into compelling messages to help physicians best serve their patients

  • Able to develop peer-to-peer relationships with top ranking healthcare professionals

  • Able to develop good collaboration with business partners and work cross border

We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled