Scientific Advisor Oncology

**Working with Us**Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley.**Role Summary**:Scientific Advisors embody our medical mission by becoming a trusted, agile partner who engages in influential dialogue and deliver timely, high impact data and insights that advance science or accelerate access, shape medical practice, and drive appropriate adoption of BMS medicines.The **Scientific Advisor, Oncology** role is a blend of field-based and office-based time; the proportion depending on the life cycle for the compound/therapeutic area of responsibility. It is anticipated that a scientific advisor fulfilling their internal and external duties will spend a minimum of **60 percent of their time in the field** with external customers. SAs will perform their activities in an ethical and compliant manner, in adherence with all BMS policies and external laws and regulations. The Scientific Advisor is responsible for actively engaging with Thought Leaders and to serve as the Therapeutic Area (TA) reference point within their geographic scope. The SA is responsible to design and deliver the medical plan, provide medical support to internal matrix partners, and foster effective and open relationships with the partners. Support the development Brand Strategies in collaboration with BMS commercial.**Key Responsibilities****Medical Planning/Executions**- Develops capabilities to enable delivery of quality medical and strategic stewardship and to ensure simplification.Evaluates business processes and initiatives to determine appropriate interventions that meet departmental goals.- Collaborates with colleagues across business units and medical areas to ensure a streamlined approach to best practices and innovative ideas regarding promotional materials.- Oversees and interprets new scientific data, literature, competitive trends and product opportunities and adjusts medical and educational activities accordingly.- Serves as a medical and technical resource for clinical issues raised by internal and external collaborators, investigators, consultants, patients and contract resources.- Establishes partnership with patient organizations, professional organizations and medical societies to understand their unmet medical needs.**External Environment and Customer Focus**- Profile the medical landscape in the country 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.- Develop and maintain Thoughts Leaders-TLs/Health Care Professionals-HCPs engagement plan.- Contribute to involvement of TLs in local and/or Global Development Organization-GDO driven studies, Compassionate Use Program-CUP/Early Access Programs-EAPs and other scientific activities.- Effectively 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.- Provide scientific information to and collaborate with relevant local functions.**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 supervising and coordinating 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 participates in the review process of Risk Minimization Materials/ARMA materials.**Compliance**- Endorse and implement a cul