AbbVie
Assistant Director, Scientific Medical Affairs
Join to apply for the
Assistant Director, Scientific Medical Affairs
role at
AbbVie Assistant Director, Scientific Medical Affairs
Join to apply for the
Assistant Director, Scientific Medical Affairs
role at
AbbVie This range is provided by AbbVie. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range
$137,500.00/yr - $261,000.00/yr Company Description
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. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Seniority level
Seniority level
Director Employment type
Employment type
Full-time Job function
Job function
Health Care Provider Industries
Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at AbbVie by 2x Sign in to set job alerts for Director Medical Affairs roles.
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Join to apply for the
Assistant Director, Scientific Medical Affairs
role at
AbbVie Assistant Director, Scientific Medical Affairs
Join to apply for the
Assistant Director, Scientific Medical Affairs
role at
AbbVie This range is provided by AbbVie. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range
$137,500.00/yr - $261,000.00/yr Company Description
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. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Seniority level
Seniority level
Director Employment type
Employment type
Full-time Job function
Job function
Health Care Provider Industries
Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at AbbVie by 2x Sign in to set job alerts for Director Medical Affairs roles.
Social Media Strategy & Content Assistant Manager
New York City Metropolitan Area $80,000.00-$85,000.00 1 week ago New York City Metropolitan Area 3 weeks ago Assistant Manager, Commercial Planning and Operations
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New York, NY $100,000.00-$135,000.00 1 week ago Assistant Manager, Amazon E-Commerce Marketing
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