Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline (Lung Cancer)

AbbVie•Mettawa, IL

22h•Hybrid

About The Position

The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient’s journey. The Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline provides medical and scientific input into core strategic and operational pipeline medical affairs activities for the lung cancer portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with sales, marketing, and commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.

Requirements

Scientific Director Qualifications: Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred.
Typically, 10-15 years of experience in the pharmaceutical industry or equivalent
7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
Substantial knowledge of relevant therapeutic area required.
Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
Proven leadership skills in a cross-functional global team environment.
Must possess excellent oral and written English communication skills.
Senior Medical Director Qualifications: Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D).
Relevant therapeutic specialty in an academic or hospital environment preferred.
Completion of residency and/or fellowship is preferred.
Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent.
3+ years of experience is preferred.
Substantial knowledge of relevant therapeutic area required.
Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
Proven leadership skills in a cross-functional global team environment
Ability to interact externally and internally to support global business strategy.
Must possess excellent oral and written English communication skills.

Responsibilities

Leads medical input into disease area strategy and asset strategies within the lung cancer oncology pipeline portfolio.
Leads pipeline medical evidence generation strategy and execution including company sponsored studies, research collaborations and investigator initiated studies.
Provides in-house medical expertise for the disease area and assets, coordinating appropriate scientific activities with internal and external stakeholders as they relate to ongoing programs.
May participate in due diligence or other business development activity as required by program needs, and contribute to translational strategy in partnership with discovery colleagues.
Acts as a medical interface and actively solicits insights and opinion through the development and execution of medical expert engagement strategies, partnering with clinical development, commercial, access, area and affiliate colleagues to ensure that broad perspectives both internally and externally are incorporated into strategies and plans as appropriate.
Leads creation of early scientific narratives, messaging, and communications activities including congress planning, medical education, publication strategies and plans.
May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.
Assists with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
May interact with and coordinates 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.
Serves as the scientific team interface for key regulatory discussions.
Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information.
Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.