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: 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. Southeast region will include: Florida, Alabama, Puerto Rico 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 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 oral communication skills are imperative; strong interpersonal skills commensurate with the need to collaborate closely with partners, investigators, contractors, consultants, and team members across functions. - Established track record of effective and influential oral presentations to both large and small audiences within the healthcare profession. - Ability to complete required training, documentation, expense reporting, and other administrative tasks. - Willingness and ability to travel 50-70% including overnight stays. - Ability to manage a geographically assigned territory from a home-based office. - Computer skills including Excel, Word, Power Point, Outlook, and programs such as Zoom are expected. - Valid driver’s license - Doctorate level or 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 - Prior pharmaceutical industry experience as a MSL/RSD with solid understanding of scientific exchange in the context of compliance/ regulated environment and robust experience supporting execution of clinical trial. - Therapeutic knowledge in allergy/immunology/HAE, cardiology/ATTR-CM/-PN, or genetic medicine highly preferred. - New product launch experience highly preferred. - Ability to sit or stand for multiple hours at a computer - Manual dexterity for keyboarding; may include repetitive movements #LI-Remote 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 base salary for this position is expected to range between $216,000.00 - $264,000.00 USD per year.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.

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: 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. East Central region will include: Ohio, Pennsylvania, New Jersey, West Virginia 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 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 oral communication skills are imperative; strong interpersonal skills commensurate with the need to collaborate closely with partners, investigators, contractors, consultants, and team members across functions. - Established track record of effective and influential oral presentations to both large and small audiences within the healthcare profession. - Ability to complete required training, documentation, expense reporting, and other administrative tasks. - Willingness and ability to travel 50-70% including overnight stays. - Ability to manage a geographically assigned territory from a home-based office. - Computer skills including Excel, Word, Power Point, Outlook, and programs such as Zoom are expected. - Valid driver’s license - Doctorate level or 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 - Prior pharmaceutical industry experience as a MSL/RSD with solid understanding of scientific exchange in the context of compliance/ regulated environment and robust experience supporting execution of clinical trial. - Therapeutic knowledge in allergy/immunology/HAE, cardiology/ATTR-CM/-PN, or genetic medicine highly preferred. - New product launch experience highly preferred. - Ability to sit or stand for multiple hours at a computer - Manual dexterity for keyboarding; may include repetitive movements #LI-Remote 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 base salary for this position is expected to range between $216,000.00 - $264,000.00 USD per year.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.

We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger – helping to simplify health care one person, one family and one community at a time. Do you have a passion for engaging with people and helping them on their journey to better health? Signify Health, part of CVS Health®, is seeking a Part-time Physician to provide In-Home Health Evaluations, engaging with people in the comfort of their own homes and helping bridge gaps in care. In this role, you’ll be primarily traveling - up to 100% of the time - across a defined coverage area, as defined by business needs. This may require overnight hotel stays, car rentals and/or flights, depending on the prescribed coverage area. Holding multiple state licenses will be required, as dictated by business needs. You’ll play a critical role in building trusted relationships to make people healthier, helping bring flexible, comprehensive and personalized health evaluations right to people’s front doors. Job highlights The visit, which lasts about 45 minutes, allows for time to connect one-on-one and answer health questions. It includes a medication and medical history review, a physical evaluation, and, if ordered by the person’s health plan, additional diagnostic tests (i.e., diabetic eye exams, spirometry, etc.). You’ll use an iPad and an intuitive clinical workflow for each evaluation and are not required to prescribe medicine, order lab tests or alter people’s current treatment regimen. In this role, you will: - Bring your heart into every visit, joining a national network of purpose-driven clinicians dedicated to improving health outcomes - Be part of our efforts to visit millions of people nationwide with the goal of providing connections to the right care for people’s unique needs - Work with Signify Health as a clinician colleague, fulfilling the requirements of the specified role - Be flexible to travel locally and within licensed states - Conduct virtual visits as needed - Provide all Signify Health services as indicated including Diagnostic & Preventive Services products (i.e., spirometry, DEE, etc.) - Be flexible to travel locally and within licensed states A Note on Our Work Environment: As an in-home clinician, your primary workplace is the private residence of health plan members. We are dedicated to meeting health plan members where they are, wherever they call home. These environments are diverse and may present a variety of conditions. Candidates must be able to comfortably and safely perform their duties in homes that may contain household pets, secondhand smoke and other potential airborne allergens or irritants. Why Clinicians Enjoy Working with Signify Health “Many of the people I see are shocked that a physician is coming to their home to visit with them one-on-one. When you sit down and have an unhurried conversation about their health, they are impressed, happy, and understand that their health plan and care team cares about them.” - M.L., MD “The primary care physician gets a snapshot of a person in an office setting, but with Signify Health, we see things like the number of steps to enter their home, the state of disrepair those steps may be in, and the person’s ability to function comfortably and with ease in their own home. We can make referrals to the individual’s health plan, encourage the participation of their loved ones, and ensure their PCPs are aware of their health and overall quality of life.” - C.H., MD Part-time employees qualify for: - Select benefits (see benefits guide for details) - Malpractice insurance coverage (during Signify Health-related activities) - Supplies and other perks Required & Preferred Qualifications (MDs and DOs) - Active, unrestricted license(s) in coverage area(s) - Able to obtain and maintain multi-state licenses in coverage area, as required - Able to cover the following primary locations: Able to cover all counties within [state] and flex to other areas of business need This pay range represents the base pay for each In-Home Health Evaluation (and associated visit) completed by a physician. The number of In-Home Health Evaluations (and associated visits) completed per day may vary. Pay is dependent on a variety of factors including experience, education, geography and other relevant criteria. This position is eligible for other reimbursement opportunities, including pay per completed Diagnostic and Preventative Services (DPS), as ordered, in addition to the base pay listed above. Additional details will be provided. Anticipated Weekly Hours 29.5 Time Type Part time Pay Range The typical pay range for this role is: $100.00 - $100.00 This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, geography and other relevant factors. Our people fuel our future. Our teams reflect the customers, patients, members and communities we serve and we are committed to fostering a workplace where every colleague feels valued and that they belong. Great benefits for great people We take pride in our comprehensive and competitive mix of pay and benefits – investing in the physical, emotional and financial wellness of our colleagues and their families to help them be the healthiest they can be. In addition to our competitive wages, our great benefits include: - Affordable medical plan options, a 401(k) plan (including matching company contributions), and an employee stock purchase plan. - No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching. - Benefit solutions that address the different needs and preferences of our colleagues including paid time off, flexible work schedules, family leave, dependent care resources, colleague assistance programs, tuition assistance, retiree medical access and many other benefits depending on eligibility. For more information, visit https://jobs.cvshealth.com/us/en/benefits We anticipate the application window for this opening will close on: 12/31/2026 Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state and local laws.

Why ThedaCare? Living A Life Inspired! Our new vision at ThedaCare is bold, ambitious, and ignited by a shared passion to provide outstanding care. We are inspired to reinvent health care by becoming a proactive partner in health, enriching the lives of all and creating value in everything we do. Each of us are called to take action in delivering higher standards of care, lower costs and a healthier future for our patients, our families, our communities and our world. At ThedaCare, our team members are empowered to be the catalyst of change through our values of compassion, excellence, leadership, innovation, and agility. A career means much more than excellent compensation and benefits. Our team members are supported by continued opportunities for learning and development, accessible and transparent leadership, and a commitment to work/life balance. If you’re interested in joining a health care system that is changing the face of care and well-being in our community, we encourage you to explore a future with ThedaCare. Benefits, with a whole-person approach to wellness – - Lifestyle Engagement - e.g. health coaches, relaxation rooms, health focused apps (Wonder, Ripple), mental health support - Access & Affordability - e.g. minimal or zero copays, team member cost sharing premiums, daycare About ThedaCare! Summary : The Clinical Dietitian, Senior assesses nutritional status and develops and implements a comprehensive nutrition care plan. Completes nutrition focused physical assessments to accurately diagnose malnutrition. Supports writing and ordering parenteral and enteral nutrition for all hospitalized patients seven days per week. Participates in the interdisciplinary team providing care coordination, education, and support during the discharge process. Assists with planning, development, and implementation of department programs, policies, and goals. Job Description: Schedule: Day shift flexible start (7 am to 830pm) , every 8th weekend, and 1 holiday can be remote. KEY ACCOUNTABILITIES: - Develops, implements, monitors, and coordinates nutritional care plan based on assessment to client's needs with other health professionals. - Writes orders for enteral and parenteral nutrition, supplements, and additives as indicated by the assessment and plan of care. - Works seven days per week including holidays to support ThedaCare’s hospitalized patients on nutrition support (enteral and parenteral nutrition). Responds to consults within 24 hours, including patients in ambulatory settings identified with nutrition risk per nutrition risk screen. - Completes nutrition focused physical exam to diagnose malnutrition. - Counsels individuals and family members on nutritional principles, dietary plans, food selection, and economics of nutrition. Adapts plans to individual client's needs, lifestyle, and cultural eating habits. Provides follow-up and makes appropriate referrals based on needs of individual. - In collaboration with the dining and patient meal department, plans and evaluates menus to meet nutritional needs of patients with consideration for food preferences. - Documents assessments, recommendations, and plan of care in EPIC. Documents in EPIC care plans and education interventions and goals. - Participates in discharge planning. Recommends home care nutritional needs. - Interprets, evaluates, and utilizes current research to achieve effective nutritional care. - Utilizes the Nutrition Care Manuel from the Academy of Nutrition and Dietetics as a resource for educational materials. - Participates in process improvement work to support delivery of best care to patient in the acute care setting. - Oversees dietetic technician assessments and interventions per defined scope of practice per the Academy of Nutrition and Dietetics. - Serves as a preceptor for dietetic interns. QUALIFICATIONS: - Registered Dietitian - One year of experience in hospital nutrition - Certified Dietitian PHYSICAL DEMANDS: - Ability to move freely (standing, stooping, walking, bending, pushing, and pulling) and lift up to a maximum of twenty-five (25) pounds without assistance - Job classification is exposed to blood borne pathogens (blood or bodily fluids) while performing job duties WORK ENVIRONMENT: - Climate controlled office setting with daily movement throughout the facility - Interaction with department members and other healthcare providers Scheduled Weekly Hours: 24Scheduled FTE: 0.6Location: Corporate 1818 N. Meade Street - Appleton,WisconsinOvertime Exempt: NoWorker Shift Details: Days