Why Join Intellia?
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 at Intellia. We 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 With Intellia:
The Senior Medical Director will provide medical input to global clinical programs as a member of the Core team, serve as the medical expert for the study team and medical monitor for phase 1-4 clinical trials, as applicable.
Provide medical leadership for assigned Intellia clinical development programs
Partner with Clinical Program Management to develop clinical development plans (CDPs) and co-lead the clinical sub-team to execute the CDP(s)
Develop and maintain relationships with academic investigators, pharmaceutical partners/sponsors, KOL’s, and patient advocacy groups.
Contribute to activities in support of the company’s regulatory submissions, including authoring clinical sections for INDs, NDAs, and other related documents.
Partner with pharmacovigilance to best understand the safety profile of compounds.
Maintain a high level of clinical and scientific expertise in the disease area(s) by reviewing the literature, attending medical/scientific meetings, and through personal interchanges with consultants, thought leaders, investigators and internal stakeholders.
Author manuscripts and collaborate with cross-functional colleagues and thought leaders to meet publication plan objectives.
Maintain ethical standards of the highest level, with an absolute commitment to comply with all relevant ethical, regulatory, and legal strictures and the associated learnings thereof.
Lead/participate in clinical research due diligence in support of business development activity.
Interface with relevant functions (e.g. discovery, preclinical development, regulatory, clinical operations, etc.) to design and execute clinical development plans for assigned projects.
Provide medical information on existing and emerging data, in response to questions from internal and external stakeholders.
Doctoral degree (M.D.) or foreign equivalent
Completed post-graduate medical education and is US board certified (or foreign equivalent) in a medical specialty in gene therapy or metabolic disease strongly preferred.
3 to 8 years of direct pharmaceutical drug development experience required in the biotech/pharmaceutical industry
Must have multi-trial, Phase 2/3, global experience
Experience in multiple therapeutic areas or disease state/indications desirable, including life cycle management.
Knowledge and experience in gene therapy, rare disease, and oncology preferred
Experience running complex clinical research programs
Team player with commitment to cross-functional working and yet, fully capable of independent working
Proven leadership through respect, example, knowledge and influence
Excellent communication and presentation skills
EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.