Scientific Director/Senior Medical Director, Global Medical Affairs Precision Medicine

Key Responsibilities

• Develop and execute the Global Medical Affairs Precision Medicine strategy supporting AbbVie's oncology portfolio.
• Build scalable capabilities in companion diagnostics, biomarkers, digital pathology, AI-enabled diagnostics, liquid biopsy, and emerging technologies.
• Establish strategic partnerships with IVD companies, pathology societies, academic institutions, reference laboratories, and technology partners.
• Lead global evidence generation, medical education, scientific communications, and pathology congress strategies supporting biomarker adoption.
• Partner cross-functionally to ensure diagnostic strategies are integrated into clinical development and commercialization plans.
• Evaluate emerging technologies and external collaborations that strengthen AbbVie's precision medicine capabilities.
• Serve as the Medical Affairs precision medicine representative on global cross-functional teams and provide scientific leadership to internal and external stakeholders.

Qualifications

• Position will be commensurate with experience.
• Scientific Director: Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred. Typically, 10-15 years of experience in the pharmaceutical industry or related. 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
• Senior Medical Director: Medical Doctorate (M.D.) 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 preferred. Minimum 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 5 years of experience is preferred.

Qualifications: Substantial understanding of relevant therapeutic area required.

• Substantial understanding of relevant therapeutic area required.
• Direct subject matter expertise in multiple myeloma 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 cross-functional global team environment.
• Able to interact externally and internally to support global business strategy.
• Excellent oral and written English communication skills.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits allocable to a particular employer remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

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.

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