Assistant Director, Scientific Medical Affairs

The Assistant Director Medical Affairs has a key role within the designated Therapeutic Area. Working under the leadership of the Scientific Director/Medical Director this leader supports the development and execution of the therapeutic area medical strategy specifically as it pertains to the specific asset or indication by providing scientific strategic and operational input into core medical affairs activities including thought leader engagement plans and field provider interactions; generation and dissemination of clinical and scientific data; provider and payer educational initiatives and  promotional material generation this leader ensures tactical execution is relevant to the market physicians patients and payors. 

Responsibilities 

• With oversight contributes to the development of the Oncology/Hematology therapeutic area strategy.  

• Contributes to the development of and leads the execution of the medical education tactics advisory boards and thought leader engagement plan in line with the indication or assets strategic plan. 

• Leads conference planning and execution. Represents AbbVie at external meetings including investigator meetings scientific association meetings etc. 

• May be responsible for Medical Review (MR) training for on label clinical data and disease state. 

• Responsible for managing budget for assigned projects including consulting and vendor management. 

• Supports clinical and scientific data generation including alignment of the Investigator Initiated Study (IIS) strategy as needed to support external communication 

• Provides subject matter expertise for commercial teams including competitive assessments and regular scientific literature reviews. 

• Aligns medical education and scientific initiatives with the Scientific Communication Platform. 

• Contributes to the generation of Medical Information (MI) communication content and supports training on MI materials. 

• Contributes to all launch readiness reviews/planning. 

Qualifications :

• Scientific degree; advanced degree (e.g. MS PhD MD/DO PharmD NP MSN) preferred. 
• 3-5 years of clinical scientific/research or industry related experience or equivalent required demonstrating strong leadership competencies and proven team-building skills with ability to lead in a global matrixed environment. Substantial understanding of relevant therapeutic area required. 
• Good understanding of legal and regulatory guidelines (e.g. knowledge of OPDP promotional regulations CDER/CBER regulations as they relate to drug approvals). 
• Good understanding of Good Clinical Practices ICH guidelines PhRMA code FDA CFR ISO clinical research ethics HIPAA and patient privacy laws EU Directive and other applicable local regulations 
• Good understanding of Medical Affairs principles study design and publications. 
• Knowledge of clinical trial methodology regulatory requirements governing clinical trials and experience in the design of protocols preferred. 
• Interactions normally require the ability to gain cooperation of others conduct presentations of technical information concerning specific projects and schedules etc. 
• Ability to interact externally and internally to support global business strategy. Ability to work effectively with different cross functional groups and have strong interpersonal and communication skills.  
• Able to coordinate appropriate scientific and medical activities with internal stakeholders (i.e. commercial clinical operations discovery statistics regulatory etc.) as they relate to on-going medical affairs projects.  
• Ability to work effectively in a team/matrix environment. Ability to influence others without direct reporting relationships. 

• Preferred:

• Expertise in the therapeutic area of Oncology/Hematology.

Additional Information :

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. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

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