This position sits onsite 3 days weekly (2 days remote) at our North Chicago, IL headquarters or Madison, NJ site.

　　Responsibilities:

　　Identifies Insight Trends: Address educational scientific gaps identified through the gathering of feedback from multiple field sources, compile and summarize to provide relevant insights. Communicate trends to the broader therapeutic team.

　　Translates integrated brand plan into medical tactics and core communication topics: Responsible for designing a strategically aligned tactical plan, as appropriate for on market products, and pipeline products including new indications/disease states. Develops non-promotional field/affiliate resources and ensures communications are supported by medical communication standards, pharmacovigilance standards, SOP’s and all other quality and compliance standards in Medical Affairs.

　　Provides input into externally facing materials for use : (i.e. Congress Booth, Ad Boards, Med Ed) with HCP or EE interactions (Payer, Patients, Prescribers, and Providers); educational initiatives (medical education, data, guidelines, and value proposition)

　　Identifies, Designs and implements focused and impactful internal training programs: aiming to shape scientific understanding and medical practice (e.g. for Sales Representatives, MSLs, MOSLs, Affiliates)

　　Promotional Material Review: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials for assigned therapeutic area(s) within Medical Affairs. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs.

　　Actively contributes to medical and brand functional planning including: medical education, EE engagements; and provides strategic medical input into core brand/product strategies. Works with TA Lead to ensure external communication strategies and tactics align with both TA and Commercial Strategies

　　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.

　　Knowledge of clinical trial design, results and methodology, regulatory and compliance requirements governing development of promotional and non-promotional materials is desirable.

　　Ability to interact externally and internally to support global scientific and business strategy.

　　Ability to independently evaluate risk and implement strategies that are compliant with applicable regulatory standards pertinent to the promotion of pharmaceutical products

　　Demonstrated analytical, conceptual and administrative skills. Excellent communication skills (written and presentation).

　　Flexibility and adaptability to organizational change and market demands. Ability to work in a fast-paced corporate environment. High sense of urgency and commitment to excellence in the successful achievement of objectives.

　　Excellent planning and organizational skills. Ability to manage multiple priorities and ability to demonstrate good business judgment.

　　Strong Project Management and Teamwork skills to address project risks and issues.

　　Ability to influence without direct authority to effectively deliver cross-functional projects

　　AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.