Regional Scientific Director, Lakes Region

Position: Regional Scientific Director, Great Lakes Region
Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.

Beyond our science, we live our four core values:
One, Explore, Disrupt, Deliver and feel strongly that you can achieve more  have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done.

We want all of our people to go beyond what is possible. We aren’t constrained by typical end rails, and we aren’t out to just “treat” people. We’re all in this for something more. We’re driven to cure and motivated for change. Just imagine the possibilities of what we can do together.
** How You Will Achieve More:
** The Regional Scientific Director (Associate Director level) serves in a customer-facing medical role to establish trusted partnerships within the healthcare community covering Intellia’s CRISPR-based, first-in-class gene editing programs.  Key responsibilities include scientific exchange, medical education and insight identification with PIs, KOLs, healthcare multidisciplinary teams and referral HCPs.  RSDs will support both the nex-z and lonvo-z programs.

Great Lakes region will include:
Michigan, Minnesota, Wisconsin, North Dakota, South Dakota, Madison, Milwaukee
** Responsibilities:
** The RSDs will focus their engagement efforts to KOLs and trial sites providing the following:

Scientific Engagement Activities
* Engagement with KOLs across ATTR amyloidosis and HAE within territory to provide education on our CRISPR gene editing platform and reactively educate on the MoA and clinical data on nex-z and lonvo-z.
* Understanding of patient journey at key centers and identification of site capabilities and preferences regarding gene editing.
* Development of individualized scientific engagement plans for key KOLs aligned with scientific narrative and medical strategy.
* Identify external insights and knowledge gaps through listening for key intelligence topics of interest and timely reporting via CRM
* Medical Congress attendance to enable KOL engagement, medical booth staffing, scientific session coverage, insights gathering and reporting
* Institutional presentations on Intellia scientific evidence, as appropriate.

Clinical Trial Awareness and Enrollment Focused Activities
* Provide scientific support for Phase 3 clinical trials during site start up, activation and recruitment through scientific education and operational insights
* Establish, cultivate, and maintain scientific relationships with Investigators and study site teams
* Identify barriers to site activation and/or patient recruitment, and discuss solutions with Investigators, study site teams, and institutional administrative team members to address and remove these barriers.
* Escalate site feedback or concerns to Intellia clinical teams
* Develop a robust understanding of clinical practice and referral associated with gene editing therapies.
* Ensure compliance and high level of scientific integrity in all interactions, including completion of trainings on time and adherence to policies
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* About You:

*** Demonstrated success working in a highly matrixed, cross-functional environment.
* Ability to critically assess situations to prioritize the importance, urgency and risks, and present leadership with recommendations.
* Ability to anticipate change and to flexibly adapt to changing business needs.
* Self-starter and team player with a collaborative spirit and results orientation.
* Organized, able to multi-task to meet timelines in a fast-paced environment with strong attention to accuracy and detail.
* Excellent presentation, communication, and project management skills across a variety of interaction mediums including in person, digital, email, phone, etc.
* Ability to understand and clearly and effectively communicate complex scientific and medical information to both internal and external stakeholders.
* Excellent written and…