Head of Asset, Medical Affairs - Gastroenterology

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Leads the Gastroenterology team in developing and executing the Medical Affairs strategy for  Upadacitinib.  Responsible for practical and clinically meaningful data strategy and delivery to inform clinical use and transform standard of care.  Aligning all internal parties on Medical Benefit-Risk Evidence based positions.  Deeply understanding the patient journey and apply insights into determining the medical need.  Expected to work closely with Clinical Development and Asset Teams to ensure that global customer insights and health care practices, current and future are incorporated in the clinical development and regulatory plans.  Provide strategic medical input into core brand strategies, and to support medical marketing activities and market access.     

Responsibilities: 

•Actively participates in advancing and communicating corporate and GMA philosophy and agenda. Participates as a member of TA Management.  Coordinates induction, mentoring, training, and development of team.  Identifies training needs. May supervise 2-10 employees, including other MDs or PhDs.  Responsible for all aspects of talent management for own team and provides feedback as part of TA management.  May assist in developing/mentoring junior medical affairs staff.
•Participates in design and execution of clinical trial safety, product safety and risk management plans.  May also carry responsibility for routine and adhoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE’s) and Serious Adverse Events (SAE’s) if assigned to AbbVie conduct on clinical studies.
•Oversees the conduct of clinical trials and is medically and scientifically accountable for resolution of safety (AE’s & SAE’s) issues, interpretation of statistical analyses for clinical significance, PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities.
•All clinical research / development activities for products under development, and for post approval commitments such as regulatory agency mandated trials, or those intended to support product registration or to generate data for label inclusion remain the primary responsibility of TA development teams.  Assists with the scientific review, development, approval, execution and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
•Drives medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy.  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.
•Oversees scientific/medical education of 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.  May develop scientifically accurate marketing materials, medical education programs, advisories, and symposia.  Maintains an up-to-date analysis of competitor product information.
•May act as consultant/liaison with other corporations when working under licensing agreements and/or in the evaluation of new business development opportunities. Represents AbbVie at external meetings including investigator meetings, scientific association meetings, etc.  May act as medical/scientific leader for several programs within an area.  May represent the medical function on cross-functional integrated teams for medical affairs activities.
•Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as the scientific team interface for key regulatory discussions.
•Drives Medical Affairs strategies and