Associate Director, Healthcare Compliance
- Employer
- Intellia Therapeutics
- Location
- Cambridge, MA
- Posted date
- Sep 28, 2026
View more categories
- Discipline
- Regulatory, Legal/Compliance
- Required Education
- Associate Degree
- Position Type
- Full time
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Job Details
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 wantall ofour 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 Associate Director, Healthcare Compliance, will play a critical role in building and supporting Intellia’s Healthcare Compliance Program in connection with the commercialization of Intellia’s first product, a gene editing therapy for hereditary angioedema (HAE).
This role will build, implement, and continuously improve Intellia’s Healthcare Compliance Program across a range of areas with a focus on monitoring, risk and compliance assessments, and transparency reporting through close partnership with the Commercial and Medical Affairs organizations, cross-functional collaboration, and a collective commitment to uphold Intellia’s integrity.
This role will report to the Senior Director of Healthcare Compliance. This role requires strong initiative, a willingness to take on complex initiatives, and a desire to provide support across a fast-paced organization preparing to launch a novel therapy.
Responsibilities:
Develop and lead the annual risk-based monitoring plan as informed by ongoing risk assessments and emerging compliance needs.
Partner cross-functionally to facilitate auditable record-keeping.
Oversee and conduct live and transactions monitoring activities leveraging new and emerging technologies to drive efficiency and accuracy (e.g., AI solutions).
Identify trends, gaps, and areas for improvement, and report to senior leadership.
Work closely with Legal and Healthcare Compliance colleagues to conduct risk and compliance assessments.
Lead and manage the project lifecycle for compliance project initiatives
Maintain understanding of Intellia’s business objectives and activities and keep abreast of industry and enforcement trends that may impact Intellia’s operations and Healthcare Compliance Program.
Serve as Intellia’s subject matter expert on the Physician Payments Sunshine Act and related aggregate spend reporting and state transparency reporting requirements.
Partner cross-functionally to oversee the collection and compilation of reportable transactions, and reporting to national and state authorities.
Promote Intellia’s values and establish “Compliance by Design” principles as integral to achieving business objectives and improving processes and decision-making.
As part of a growing and evolving business, this role will have the opportunity for a diverse workload, visibility to senior leadership, and continued development opportunities.
About You:
Unimpeachable integrity, good judgment, assertiveness, an approachable demeanor, and the ability to elicit the respect and trust of employees
General knowledge of pharmaceutical laws, regulations and industry guidance pertaining to the commercialization of biopharmaceutical products
Experience in the biopharmaceutical industry and understanding of key commercial activities, including sales and marketing, HCP and patient engagements and interactions, and patient support services; launch experience and experience in rare disease is a plus
Self-starter who can lead projects independently from inception to completion with minimal supervision
Excellent communications skills, both verbal and written, including the ability to effectively lead presentations and deliver trainings
Exceptional organizational skills and attention to detail
Solid track record of building strong working relationships in a cross-functional matrix environment, working with different personality types, and managing conflict
Strong work ethic, positive outlook, commitment to legal and business teams
Collaborative style; team player
Education / Certifications
B.A./B.S. degree required
Experience
6+ years of healthcare compliance and/or other related experience in a commercial stage biotech/pharmaceutical organization
Physical Requirements
Prolonged periods of sitting at a desk and working on a computer
Ability to travel 15-20%
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.
Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down.
The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors.
Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company’s discretion.
For more information about Intellia’s benefits, please click here.
Company
Many of us pursuing work in the biotechnology industry are inspired by a loved one who is living with a disease or the loss of someone in our community. Rare genetic and oncological and immunological diseases not only affect the people living with often debilitating and life-threatening symptoms, but these disorders also significantly impact their families, friends and caregivers.
Our researchers work tirelessly to harness the genome editing technology CRISPR/Cas9 for human therapeutic use. Jennifer Doudna, an Intellia co-founder, and Emmanuelle Charpentier were awarded the 2020 Nobel Prize in Chemistry for their pioneering work in CRISPR. We at Intellia are humbled to have a hand in making what we believe to be medical history. As a leader in this space, we take this responsibility to patients seriously.
We are employing a modular genome editing platform to create diverse in vivo and ex vivo pipelines, spanning a range of therapeutic indications. Guided by this full-spectrum approach, we are committed to making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to creating novel engineered cell therapies for various cancers and autoimmune diseases.
Change life stories with genome editing therapies!
Stock Symbol: NTLA
- Phone
- (857) 285-6200
- Location
- 400 Technology Square
Suite 100
Cambridge
Massachusetts
02139
