Cerebral and Resilience Lab have joined forces to build a new standard in mental health care—one that emphasizes better outcomes through stronger clinical decision-making, rigorous training, and professional excellence. By combining Resilience Lab’s Methodology & clinically-led training Institute with Cerebral’s extensive reach, clinical network, and care capabilities, we are creating a national model for high-quality, integrated, and accessible behavioral health care. We believe quality mental health care starts with curiosity, professionalism, and mastery of clinical decision-making. Joining our team means committing to show up on your best foot every day where you’ll be equipped with structured training, supportive supervision, and a methodology designed to guide you in making sound clinical decisions. The Role: We are hiring a Direct Care Psychiatrist! Cerebral provides evidence-based treatment for adults seeking mental health care. Our telemedicine prescribers collaborate with Therapists and Psychiatrists to support clients during their mental health journey. This role provides direct patient care for a panel of clients and allows for flexibility when client sessions can be scheduled. You can see clients during traditional business hours, evenings, or on weekends. This position is a 1099 independent contract role. Who you are: - Hold an active MD/DO license in good standing in Tennessee - National Board Certification in Psychiatry - DEA license - Comfortable assessing and formulating evidence-based treatment plans for clients with mental illness - Maintain a strong evidence-based clinical skill set while practicing & implementing outcome-focused care - Empathetic and intuitive listening - Strong verbal and written communication - Knowledgeable in crisis response - Comfortable working autonomously in a telemedicine environment - Tech-savvy with the ability to navigate various systems & tools with ease (this includes, but is not limited to Google Workspace, proprietary EMR, etc.) - Passionate about our mission of improving access to high-quality mental health care - An entrepreneurial spirit or previous experience within a startup or fast-paced environment is preferred How your skills and passion will come to life at Cerebral: - Hold thoughtful and engaged sessions with clients; 40 minute initial sessions and 20 minute follow up sessions - Provide a minimum of 15 hours of weekly availability - Create your own flexible schedule based on your individual availability! Scheduled time must fall within the hours of 6:00am to 11:30pm per your specific timezone - Must be clinically strong, function autonomously and competently, and utilize critical thinking skills to provide appropriate care - You will work collaboratively with other mental health care partners at Cerebral to ensure the most beneficial level of treatment for our clients - Work alongside other like-minded clinicians that have a common goal to positively impact the lives of others, and create an environment that leads to favorable outcomes for clients What we offer: - Mission-driven impact: - Shape the future of the #1 largest and fastest growing online mental health care company in the world - Build a platform that is improving the lives and well-being of hundreds of thousands of people - Join a community of high achievers who have a passion for promoting mental health - Path to develop & grow: - Readily available psychiatrists and clinician leadership for case consultations to ensure you always receive the support you need - Access to innovative technology to support you in delivering the highest quality of care to your clients - Access to UpToDate for continued education (free CEU offering) - Remote-first model: - Flexibility to choose the hours and schedule that work best for you - Work virtually from anywhere in the United States - Culture & connectivity: - Highly-responsive and supportive team of clinical and operational management - Decreased administrative time for clinicians through ongoing technology improvements and automations - Fully integrated, data-enabled EMR with embedded clinical decision support, monthly prescriber metric reports, and task management system - Opportunity to participate in strategic development initiatives to improve our clinical quality and safety and/or clinical processes across the organization Who we are (our company values): - We Deliver Client Impact: Relentlessly focusing on advancing personalized, high-quality, evidence-based care that improves people's lives - We are One: Bringing our collective expertise together as a unified team, strengthened by collaboration, trust, diversity of thought and shared purpose - We Aim Higher: Continuously curious to drive our learning, our innovation and our personal growth to reach our full potential - We are Generous: Giving more than we take with compassion, empathy, support, openness and a willingness to help those in need - We are Accountable: Acting with courage, conviction and integrity to achieve our goals and ambitions to improve the lives of our clients Cerebral is committed to bringing together humans from different backgrounds and perspectives, providing employees with a safe and welcoming work environment free of discrimination and harassment. As an equal opportunity employer, we prohibit any unlawful discrimination against a job applicant on the basis of their race, color, religion, gender, gender identity, gender expression, sexual orientation, national origin, family or parental status, disability, age, veteran status, or any other status protected by the laws or regulations in the locations where we operate. We respect the laws enforced by the EEOC and are dedicated to going above and beyond in fostering diversity across our workplace. ___________________ Cerebral, Inc. is a management services organization that provides health information technology, information management system, and non-clinical administrative support services for various medical practices, including Cerebral Medical Group, PA and its affiliated practices (CMG), who are solely responsible for providing and overseeing all clinical matters. Cerebral, Inc. does not provide healthcare services, employ any healthcare provider, own any medical practice (including CMG), or control or attempt to control any provider or the provision of any healthcare service. “Cerebral” is the brand name commonly used by Cerebral, Inc. and CMG.

• Lead the formulation and implementation of the Clinical Development Plan • Work with CRO medical monitors and sites to review and respond to site queries • Ensure successful completion of trial-related documents with cross-functional team members • Analyze, evaluate, interpret, and report clinical data • Contribute to drafting and reviewing of clinical documents and regulatory submissions • Provide clinical science related leadership to study teams • Responsible for high quality collaboration with external stakeholders • Contribute to regulatory strategy and maintain up-to-date knowledge

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.