US/Global Medical Director/Scientific Director, Hematology, Multiple Myeloma

Responsibilities

• Initiates medical affairs activities, generation and dissemination of data supporting the overall scientific strategy.
• Responsible from Global Medical Affairs for the design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.
• Screens, selects and drives the execution of investigator initiated studies and is responsible for oversight of study enrollment and overall timelines for key deliverables.
• May lead delivery of scientific alignment plan, brand plan, and integrated tactical plan. Develops innovative research concepts for clinical data generation; provides relevant scientific and technical training to internal teams globally
• Drives medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy. Coordinates induction, mentoring, training, and development of others.
• Helps to drive the execution of the molecule and disease specific publication plan based on the unmet needs, evolving data and evolving treatment landscape through a crossfunctional collaboration with publication lead and clinical development team..
• Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information.
• 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.
• Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
• For US/Global Medical Director:
• Medical Doctorate (M.D.) degree

Benefits

Additional Information

Provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and 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.

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Company Intel

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