Regional Scientific Director, Southern California Region

Regional Scientific Director (Associate Director level) — Responsibilities:
- Establish trusted partnerships across the healthcare community covering Intellia’s CRISPR-based gene editing programs (supports both nex-z and lonvo-z)
- Engage KOLs across ATTR amyloidosis and HAE to provide education on the CRISPR gene editing platform and reactively educate on mechanism of action and clinical data
- Understand patient journey at key centers; identify site capabilities and preferences regarding gene editing
- Develop individualized scientific engagement plans aligned with scientific narrative and medical strategy
- Identify external insights and knowledge gaps through listening; report timely insights via CRM
- Attend Medical Congresses to enable KOL engagement, staff medical booths, cover scientific sessions, gather and report insights
- Deliver institutional presentations on scientific evidence as appropriate
- Provide scientific support for Phase 3 clinical trials during site start-up, activation, and recruitment
- Establish, cultivate, and maintain scientific relationships with Investigators and study site teams
- Identify and help resolve barriers to site activation and/or patient recruitment (with Investigators, site teams, and institutional administrative teams)
- Escalate site feedback or concerns to Intellia clinical teams
- Maintain compliance and scientific integrity, including timely completion of required trainings and adherence to policies
- Develop a robust understanding of clinical practice and referral associated with gene editing therapies

Qualifications (Required):
- Doctorate level/terminal degree (Pharm.D., Ph.D., M.D. or D.O.)
- 3+ years industry or related field experience
- Extensive clinical trial experience including Phase 3 trials
- Valid driver’s license
- Ability to travel 50–70% (including overnight stays)

Skills/Qualifications (Preferred):
- Prior pharmaceutical industry experience as a MSL/RSD with knowledge of scientific exchange in a compliance/regulatory environment and experience supporting clinical trial execution
- Therapeutic knowledge in allergy/immunology/HAE, cardiology (ATTR-CM/ATTR-PN), or genetic medicine
- New product launch experience

Application instructions:
- Applications are accepted on a rolling basis until the position is filled.