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Director II, Precision Medicine Oncology Leader

1 month ago


Waltham, Massachusetts, United States AbbVie Full time
Job Summary

We are seeking a highly motivated individual with a proven track record of scientific accomplishments to join our growing Precision Medicine Oncology organization at AbbVie. As a Director, he/she will have the opportunity to work in a fast-paced and highly collaborative environment to lead the development and execution of Precision Medicine strategies for Oncology programs in early/late-stage clinical development.

Key Responsibilities
  • Lead the design, development, and execution of the overall Precision Medicine strategy for one or more AbbVie Oncology programs
  • Design and implement hypothesis-driven strategies to deliver evidence of target engagement, mechanisms of action/resistance, patient selection/CDx strategies, and other clinically relevant biomarker endpoints to advance the AbbVie Oncology pipeline
  • Enable cross-functional collaboration on the Precision Medicine strategy, leading the design, execution, analysis, communication, and publication of translational research and correlative clinical biomarker studies
  • Author and review Precision Medicine related sections in clinical study/regulatory documents
  • Ensure that overall budget, schedule, and performance standards are attained, and be accountable for the overall Precision Medicine strategy in oncology clinical studies, in compliance with AbbVie's processes and regulatory requirements
Qualifications
  • PhD, MD, or PhD/MD degree in a relevant scientific field (e.g. cancer biology, cancer genetics, molecular oncology, cell biology) with 10+ years of relevant experience in the pharmaceutical industry or equivalent
  • Strong scientific background in oncology. Expertise in ovarian cancer, other solid tumors, and/or antibody drug conjugates highly desirable
  • Demonstrated leadership in development and execution of translational research and clinical biomarker strategies in early and/or late clinical development in oncology
  • Experience leading cross-functional teams responsible for developing/implementing Precision Medicine strategies for oncology programs in a drug development setting
  • Knowledge of clinical trial methodology, regulatory requirements governing clinical trials, companion diagnostics, protocol design, and/or experience in clinical development strategy preferred
  • Strong passion to drive clinical innovation through Precision Medicine to improve outcomes for patients with cancer
  • Excellent written and oral communication skills, strong organizational skills with attention to detail, and effective time management with an ability to distill complex issues and clearly articulate/present solutions
  • Strong interpersonal and collaboration skills to work in a team-oriented, matrix environment, and the ability to interface with multiple cross-functional stakeholders