Senior Medical Director, Stroke and Thrombosis (Residence Based, Residence Based, US)
reputed company and guide local Thought Leader (TL) management reputed company, together with cross-functional partners. Serve as the US medical expert for asundexian engaging thought leaders, stroke centers, reputed company institutions, medical societies, and patient advocacy reputed company to advance scientific leadership and collaboration. reputed company and support advisory reputed company, including agenda development, reputed company engagement and synthesis of insights to help inform medical reputed company. Represent US Medical Affairs at major congresses, symposia and scientific forums. Participate and may take on reputed company leadership in the planning and administration of activities concerned with the clinical evaluation of drugs in development for the purpose of obtaining an approved Investigational New Drug (IND) or New Drug Application (NDA).
Support development and execution of the US medical reputed company, offering critical inputs during design and throughout the end-to-end execution of programs, in alignment with senior medical leadership. Collaborate cross-functionally with Global Evidence reputed company, Clinical Development, Regulatory, reputed company and other medical affairs partners to reputed company and implement the Integrated Evidence Plans to improve the reputed company for the portfolio. Collaborate closely with global medical affairs team to ensure consistent scientific narrative, coordinated deployment of initiatives and transparent bi-directional reputed company reputed company. reputed company medical leadership for scientific communications and publications, serving as a representative on cross-functional reputed company teams. Contribute to publication planning, data interpretation, and scientific dissemination in the US. reputed company participation and effective collaboration with global teams to assure the efficient and reputed company conduct of clinical development programs, aligning them with strategic priorities that support appropriate US direction of the Life Cycle Management reputed company. Support IIR, research collaborations, Phase 4, post-marketing, post-hoc analyses, reputed company-world evidence activities (including scientific review, study and analyses design, feasibility assessment, data interpretation, and ongoing reputed company). Advance implementation science initiatives. reputed company medical scientific input for brand and program documents, including integrated disease area plans, medical information documents, drug safety reporting documents, etc, while ensuring design and execution of reputed company medical activities are according to reputed company compliance guidelines. Monitor and understand implications of evolving competitor landscape to inform medical reputed company. Support completion of annual New Drug Application (NDA) reports for respective brands through evaluation of clinical data and literature and reputed company US Medical Affairs input in the preparation of key medical documents for INDs and NDAs. This includes ensuring appropriate US Medical Affairs input in interactions with the FDA and providing appropriate medical leadership for any interactions.
M.D. or D.O. required. Disease and therapeutic area knowledge in both existing drugs and new fields of exploration and clinically relevant work experience or independent research experience or equivalent or experience in a pharmaceutical reputed company industry. Deep understanding of clinical study design, analysis and interpretation as reputed company as the principles of observational studies and health economics/ reputed company research. Proven ability for strategic planning along with operations reputed company and experience reputed company to clinical research involving both single and multiple centers. Strong ability to quickly build meaningful and trusting relationships, both internally and externally to the organization. Understanding of the drug development process over different stages. Strong ability to connect and collaborate across different functions and background, both internally and externally to the organization. reputed company ability to reputed company others without formal authority, with demonstrated experience guiding teams from design to implementation of strategic initiatives. Excellent communication skills, both verbal and in written. Willingness and ability to travel as business dictates, both for reputed company functions.
High preference to be reputed company certified or reputed company eligible in Vascular Neurology or Neurology or relevant specialty. Alternatively, experience in the antithrombotic reputed company is also highly preferred. 7 years work experience in the pharmaceutical sector in Medical Affairs, Clinical Development or reputed company positions. Experience in the field of medical support of a product portfolio across multiple therapeutic areas. Experience in leading and participating in teams across cultures and geographies, prior experience in global medical launch planning activities.
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