Director, Digital Health Strategy [Oncology & GenMed] (Burbank)

AbbVie in Burbank, IL

  • Industry: Healthcare - Physician - Oncology
  • Type: Full Time
  • Compensation: $98,940.00 - 163,430.00 / Year*
position filled
Purpose:
As a part of AbbVie's Digital Health Function in the Development Design Center, you will have the opportunity to shape the future of clinical research. The Digital Health team is responsible for setting the strategic vision for Digital Health across the Development Organization and working across all Therapeutic Areas to bring those strategies to life in meaningful ways for AbbVie and for patients. The Director, Digital Health Strategy- Oncology & GenMed will be responsible for setting the digital health strategy and roadmap for digitally enabled endpoints across Oncology and GenMed.

Responsibilities:

  • As part of the IEST, work closely with GDLs on developing an integrated strategy for how digital health tools can unlock new value across Oncology and GenMed, including development of novel digital endpoints, health outcomes, and patient experience.
  • Serve as thought leader and trusted business advisor to clinical team leads, making sure the digital tools used ladder up to the overall evidence generation strategy.
  • Define strategic opportunities and challenges in Oncology and GenMed that AbbVie can solve with new digital health tools
  • Provide leadership to Oncology and GenMed team regarding the development of digital health strategies, device selection criteria, and efforts to maximize labeling potential.
  • Ensure endpoint strategies are aligned with bigger overall product strategic plans.
  • Provide SME input on the sections of documentation for regulatory agency meetings and participate in said meetings to address technical questions raised by regulatory agencies.
  • Help influence external stakeholders such as regulatory agencies, HTAs, advocacy groups, industry trade organizations, and investigators.


Location: Please note, this position can be based onsite at the following locations [in no particular preference] - (1) North Chicago, Illinois (2) San Francisco, California (3) Cambridge, Massachusetts.

Basic:
  • Bachelor's degree required, Preferred: Masters or higher degree in health services research, public health or related field with at least 10 years of relevant experience in a pharmaceutical industry
  • Solid understanding of the drug development process, with demonstrated experience in seeing assets progress through the pipeline
  • An understanding of the regulatory requirements for new endpoints, critical success factors and obstacles impacting device driven outcomes in successful regulatory label negotiations
  • Strong ability to collaborate with cross-functional matrix teams and external experts to influence strategies
  • Ability to influence key external stakeholders like regulatory agencies, HTA bodies and investigators
  • Excellent understanding of the changing pharmaceutical, regulatory, and technology environment
  • Strong presentation and communication skills

Associated topics: ancmg, aoa, breast, cancer, hematology, lah, oncology, palliative, physician md, physician md do

* Estimated salary


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