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About the Role
The Medical Affairs organization provides patients, healthcare providers, and payers with practical and clinically relevant information and solutions for the safe and effective use of AbbVie products. The Scientific Director / Senior Medical Director, Medical Affairs - Global Oncology Pipeline provides medical and scientific input into strategic pipeline medical affairs activities for the prostate cancer portfolio, including healthcare professional interactions, data generation, educational initiatives, and patient safety.
Responsibilities
- Leads medical input into disease area strategy and asset strategies within the prostate 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 scientific activities with internal and external stakeholders.
- Acts as a medical interface and solicits insights through medical expert engagement strategies, partnering with cross-functional colleagues.
- Leads creation of early scientific narratives, messaging, and communications activities, including congress planning, medical education, and publication strategies.
- 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 medical affairs sponsored or supported clinical research activities.
- May interact with and coordinate scientific and medical activities with internal stakeholders.
- Serves as the scientific team interface for key regulatory discussions.
- Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members.
- Keeps abreast of professional information and technology through conferences and/or medical literature.
- Ensures budgets, timelines, and compliance requirements are factored into programs' scientific activities.
Requirements
- Advanced Degree PhD or PharmD. Additional post-doctorate experience highly preferred (for Scientific Director).
- Typically, 10-15 years of experience in the pharmaceutical industry or equivalent (for Scientific Director).
- 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred (for Scientific Director).
- Substantial knowledge of relevant therapeutic area required. Direct experience and knowledge in prostate cancer strongly preferred.
- Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials, and experience in development strategy and protocol design.
- 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) (for Senior Medical Director).
- Relevant therapeutic specialty in an academic or hospital environment preferred (for Senior Medical Director).
- Completion of residency and/or fellowship is preferred (for Senior Medical Director).
- 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 (for Senior Medical Director).
- Ability to interact externally and internally to support global business strategy (for Senior Medical Director).
Skills
- Medical Affairs
- Global Medical Affairs
- Prostate Cancer
- Clinical Trial Methodology
- Data Analysis and Interpretation
- Regulatory Requirements
- Development Strategy
- Protocol Design
- Leadership
- Cross-functional Teamwork
- Communication Skills
Location
- Mettawa, IL
- Florham Park, NJ
- South San Francisco, CA
Work Type
- Hybrid
Experience Level
- 10-15 years
- 7-10 years
- 2 years
- 3+ years
Education Level
- PhD
- PharmD
- M.D.
- D.O.
Salary/Compensations
- USD 182000 - USD 346000 - yearly
Benefits
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k)
- Eligible to participate in long-term incentive programs
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