Provides specialist medical/scientific strategic and operational input into core medical affairs activities such as: health-care professional/provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines and value proposition); safeguarding patient safety (risk minimization activities / safety surveillance activities). Works closely with commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.

• Provides scientific and technical support for assigned multiple myeloma products; deliver scientific presentations; develops and maintains professional and credible relationships with, key opinion leaders; actively participate in relevant Brand Teams and helps develop medical affairs strategies for assigned multiple myeloma products; develop innovative research concepts for clinical data generation; provide relevant scientific and technical training.
• In cooperation with other medical departments, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned multiple myeloma products/projects.
• Drives medical affairs related launch activities, identifies launch risks and develops & executes mitigations strategies and makes sure that medical affairs considerations are heard during regulatory negotiations
• Drives the execution of the molecule and disease specific publication plan based on the unmet needs, evolving data and evolving treatment landscape through a cross functional collaboration with publication lead and clinical development team
• Drives Medical Affairs strategies and be a key internal contact/subject matter expert. Responsible for delivery of strategic alignment plan, brand plan, gap analysis and integrated tactical plan.
• Develops and executes innovative research concepts for clinical data generation; provides relevant scientific and technical training to internal teams globally
• Ensures appropriate selection of investigator initiated studies and maintains oversight for appropriate execution.
• Collaborates closely with HEOR and V&A team to develops and co-executes HEOR & access strategy.
• May develop of scientifically accurate marketing materials, medical education programs, advisories, and symposia
• May assist with the scientific review, development, execution and communication of area/global medical affairs sponsored or supported clinical research activities.
• Keeps abreast of evolving multiple myeloma treatment landscape as well as competitive landscape, other professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource and is able to translate this info into strategic implications.
• May lead cross functional teams in development and execution of strategic initiatives requiring integration of multiple subprojects within the therapeutic area or Medical Affairs function.
• Provides guidance to cross-functional team members to aid in the development of promotional materials. 
• Provides timely and accurate reviews of promotional strategies and tactics in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs
• Oversees the work of a small team of Scientific/Associate Scientific Directors or Medical/Associate Medical directors
• Coordinates induction, mentoring, training, and development of others. 
• Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.