BioSpace
Associate Director, Intercontinental Medical Affairs Neuroscience
BioSpace, Mettawa, Illinois, United States
Associate Director, Intercontinental Medical Affairs Neuroscience
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The Associate Director, Medical Affairs will act as the Intercontinental Neuroscience Lead, providing medical/scientific strategic and operational input into core medical affairs activities and relevant scientific and technical training to Affiliate Therapeutic Area resources. Develops and maintains professional and credible relationships with key external experts and professional societies; Provides therapeutic expertise in interactions with regulators and other external groups; Develops innovative research concepts for clinical data generation and communication. Key Responsibilities Include: Develops Area therapeutic Evidence Generation plan and Area therapeutic strategic initiatives Brings insights and knowledge from the Area into the International TA Medical Affairs strategy. Provides consultation to affiliates on the affiliate therapeutic strategy and brings insights and knowledge from the affiliates into the development of the International Medical Affairs strategy. Actively participates in cross-functional team(s), provides strategic medical input into Specialty strategies and develops medical affairs strategic initiatives for assigned products. Qualifications: Position will be commensurate with experience: Associate Scientific Director requires bachelors of science and 5-7+ years of relevant clinical or medical affairs experience in an academic, hospital, or pharmaceutical industry environment. Associate Medical Director requires an MD or equivalent and 0-2+ years of relevant clinical or medical affairs experience in an academic, hospital, or pharmaceutical industry environment. Advanced degree (MD, PhD, PharmD, DO) preferred. Extensive knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The Associate Director, Medical Affairs will act as the Intercontinental Neuroscience Lead, providing medical/scientific strategic and operational input into core medical affairs activities and relevant scientific and technical training to Affiliate Therapeutic Area resources. Develops and maintains professional and credible relationships with key external experts and professional societies; Provides therapeutic expertise in interactions with regulators and other external groups; Develops innovative research concepts for clinical data generation and communication. Key Responsibilities Include: Develops Area therapeutic Evidence Generation plan and Area therapeutic strategic initiatives Brings insights and knowledge from the Area into the International TA Medical Affairs strategy. Provides consultation to affiliates on the affiliate therapeutic strategy and brings insights and knowledge from the affiliates into the development of the International Medical Affairs strategy. Actively participates in cross-functional team(s), provides strategic medical input into Specialty strategies and develops medical affairs strategic initiatives for assigned products. Qualifications: Position will be commensurate with experience: Associate Scientific Director requires bachelors of science and 5-7+ years of relevant clinical or medical affairs experience in an academic, hospital, or pharmaceutical industry environment. Associate Medical Director requires an MD or equivalent and 0-2+ years of relevant clinical or medical affairs experience in an academic, hospital, or pharmaceutical industry environment. Advanced degree (MD, PhD, PharmD, DO) preferred. Extensive knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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