Senior Scientific/medical Director, Medical Affairs - Mettawa, United States - AbbVie

AbbVie

Verified Company

Mettawa, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Company Description
-
Position title will be based on qualifications listed below.

Leads team of scientific/medical directors and responsible for development and execution of medical strategy for HCV such as: health-care professional and provider interactions; drive focused evidence generation; educational initiatives (medical education, scientific communications, and value proposition).

As an integral core member of cross functional teams the Senior Scientific Director provides strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.

Responsibilities:

Manages team of medical affairs professionals responsible for the development and execution of medical affairs strategy for Virology, specifically HCV including LCM and line extensions
Responsible for Med Affairs strategy for Mavyret, and core Medical Affairs member of TA Leadership Team
Has overall responsibility for oversight of evidence generation together with Evidence Generation lead to ensure alignment with business strategy and evidence gaps
Colead integrated brand team and represent Medical Affairs function at different governance and cross functional meetings as appropriate (asset strategy, labeling committees, etc) and partners with other functions (commercial, market access, HEOR, Value and Access, Clin Dev etc) to ensure fully aligned cross functional strategy
Responsible for development of medical education strategies at HQ and connection with field execution and leadership
May oversee the work of assistant or associate scientific directors working on different HCV related medical projects
Acts as medical interface with external experts and stakeholders as needed and stays abreast of professional information and technology through literature, conference attendance and other sources as appropriate
Partner cross functionally to ensure value continues to be demonstrated in a rapidly evolving environment

Qualifications Scientific Director Qualifications**:

Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred
Typically, 1015 years of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required.
710 years of experience in Medical Affairs
Ability to lead team and develop medical strategy independently with little supervision.
Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
Demonstrated direct experience in strategy development and execution, evidence generation (medical/RWE and/or clinical development in the pharmaceutical industry), Medical education, thought leader management & cross functional partnership
Proven leadership skills in a crossfunctional global team environment
Ability to interact externally and internally to support global business strategy.
Demonstrated direct experience in strategy development and execution, evidence generation (medical/RWE and/or clinical development in the pharmaceutical industry), Medical education, thought leader management & cross functional partnership
Must possess excellent oral and written English communication skills.

Medical Director Qualifications:

Medical Doctorate (M.D.) degree or equivalent (D.O. or nonUS equivalent of M.D). Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship is preferred.; substantial understanding of relevant therapeutic area required.
710 years of experience in Medical Affairs
Ability to lead team and develop medical strategy independently with little supervision.
Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
Demonstrated direct experience in strategy development and execution, evidence generation (medical/RWE and/or clinical development in the pharmaceutical industry), Medical education, thought leader management & cross functional partnership
Proven leadership skills in a crossfunctional global team environment
Ability to interact externally and internally to support global business strategy.
Must possess excellent oral and written English communication skills.

Additional Information

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
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