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About the Role

The Scientific/Medical Director, Global Hematology Pipeline, Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities across the hematology pipeline. This role works closely with asset strategy, clinical development, value and evidence, and commercial teams to ensure patients, healthcare providers, and payers have the practical and clinically relevant information and solutions they need.

Responsibilities

Supports the creation and execution of disease and asset strategies.
Supports pipeline medical evidence generation strategy and execution, including company-sponsored studies, research collaborations, and investigator-initiated studies.
Leads creation of early scientific narratives, messaging, and communications activities, including congress planning, medical education, and publication strategies and plans.
Provides in-house medical expertise for the disease area and assets, coordinating appropriate scientific activities with internal and external stakeholders.
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.
Partners with clinical development, commercial, access, area, and affiliate colleagues to ensure broad perspectives are incorporated into strategies and plans.
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.
May assist in the development of 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 coordinate appropriate scientific and medical activities with internal stakeholders.
Serves as the scientific team interface for key regulatory discussions.
Ensures budgets, timelines, and compliance requirements are factored into programs' scientific activities.

Requirements

Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred.
5-7+ years of experience in the pharmaceutical industry or equivalent.
7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
Experience in multiple myeloma and cell therapies highly preferred.
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.
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.
0-2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
Ability to interact externally and internally to support global business strategy.

Skills

Hematology pipeline
Disease strategy
Asset strategy
Scientific differentiation
Value propositions
Narratives
Publication strategy
Evidence generation
Health-care professional interactions
Provider interactions
Multiple myeloma
Cell therapies
Clinical trial methodology
Data analysis
Data interpretation
Regulatory requirements
Development strategy
Protocol design
Leadership
Cross-functional collaboration
Global team environment
Oral communication
Written communication

Location

Mettawa, IL
Florham Park, NJ
South San Francisco, CA

Work Type

Hybrid

Experience Level

5-7+ years of experience in the pharmaceutical industry or equivalent
7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred
0-2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.

Education Level

PhD
PharmD
Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D)

Salary/Compensations

USD 160500 - USD 305000 - yearly

About the Company

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.

Equal Opportunity

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