Sr. Medical Director, Clinical Development Philadelphia, PA Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching the first curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA™ platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio’s headquarters and labs are located in Philadelphia, PA. For more information, please visit www.cabalettabio.com and connect with us on LinkedIn. Uniquely Differentiated. Rapid. Elegant. At Cabaletta, we are driven by the shared mission of developing cures, where a patient’s own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We’re proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work® Position Description: This role can be remote or based out of our Philadelphia, PA headquarters. East Coast candidates are preferred. Travel of 10-20% required. Cabaletta is seeking an experienced, highly motivated hands-on physician leader to serve as a Senior Medical Director, Clinical Development reporting to the VP, Clinical Development. This individual will provide the medical oversight and leadership of Cabaletta’s cell therapy programs in autoimmune diseases, including collaborating with the clinical operations, regulatory, translational research, manufacturing, and quality assurance functions; liaising with clinical investigators and site personnel; establishing and building relationships with key external experts; and interacting with Health Authority representatives, such as the FDA. The position requires a leader with significant experience working with CROs and vendors and interfacing with investigator sites to ensure operational efficiency and effective execution of trials within a complex, fast-paced environment. Key Responsibilities: - Provide medical leadership for various programs from first-in-human studies through registrational studies. Late-stage development experience is preferrable - Formulate study designs, lead protocol development, partner with internal cross-functional teams in study start-up activities, and collaborate with clinical investigators, key external experts, and Health Authorities - Participate in direct, hands-on involvement in all aspects of study conduct clinical activities, working with clinical operations, including data review, analysis, and reporting that conform to the ethical, safety, and quality standards of Cabaletta, GCP, and Health Authorities - Become an expert and remain current in the relevant therapeutic areas and in the field of cell and gene therapy through review of the scientific literature, interactions with key external experts, and attendance at relevant scientific meetings - Actively contribute during Health Authority interactions - Review available preclinical data that could inform the design of future clinical trials - Present at site evaluation and site initiation visits as applicable - In partnership with relevant cross-functional team members, actively engage in the preparation of Clinical Study Reports, Annual Reports and other safety reports, Health Authority pre-meeting packages, Investigator Brochures, periodic clinical reports, and BLA submission documents - Collaborating with cross-functional groups, formulate publication strategy including active participation in authoring, preparation and review of manuscripts, conference abstracts and presentations and other external presentations of clinical data Qualifications: - M.D., M.D./Ph.D. degree or equivalent required - Board Certification, Board Eligibility, or clinical experience in the field of Rheumatology and/or Immunology highly desirable - 7+ years of experience in clinical research, including the design and execution of complex clinical trials, with a pharmaceutical or biotech company - Experience with or exposure to the development of adoptive cell therapies or biologic therapies is desirable - Experience with Health Authority interactions and submission of clinical regulatory documents is desirable - Strong written and verbal communication skills; ability to easily engage with investigators and key external experts; and ability to effectively present at conferences, advisory meetings, and other public for a - Engaged, hands-on, independent, and goal-oriented mentality; willingness to work in highly dynamic work environment - Ability to multi-task and willingness to flexibly contribute simultaneously to multiple facets of drug development; willingness to learn new therapeutic areas and technologies - Self-motivated, innovative, and critical thinker with strong commitment to follow up on action items; strong organizational, analytical, and problem-solving skills - Strong influencing skills and ability to create a clear sense of direction - Thrives in a fast-paced small company environment and able to adjust priorities and workload based upon changing needs - Comfortable with ambiguity and ability to define processes and procedures from scratch - Strong team orientation and passion for continuous self-development - Ability and willingness to travel as required Our name – Cabaletta – is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression. For more information, please visit https://www.cabalettabio.com/join-our-crew Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm. #LI-REMOTE

ABOUT ACCOMPLISH Accomplish Health is a telehealth obesity medicine practice providing science based, stigma free personalized care. By first treating the underlying metabolic conditions including insulin resistance, type 2 diabetes, and obesity we help people to build sustainable, healthy habits while maximizing the affordability and accessibility of the care each person needs. Accomplish Health is a data-centric, objective focused, collaborative, and iterative culture where feedback and open communication are encouraged. We’re building experiences and creating clinical tools that help healthcare professionals personalize the experience for each patient. Our clinical model leverages pharmacotherapy, nutrition therapy, health coaching, and connected devices in a virtual care environment. KEY RESPONSIBILITIES - Consistently provide confidential high quality, stigma free, person-centric clinical care and a superior user experience. - Review patient intake and provide the initial patient interaction, assess and diagnose relevant disorders, and provide care plan, including the discussion of the scientific principles of obesity, the prescription of appropriate weight loss therapy based on Accomplish Health’s scientifically-based clinical protocols. - Review and manage daily tasks, patient communications, lab results. Oversee patient progress including remote physiological monitoring data. - Experience working in a team of healthcare professionals (including dieticians and health coaches) and collaborating with them to ensure positive, effective patient experiences with our organization. - Record complete, timely and legible medical records, providing appropriate encounter-related billing services. - Utilize and support a detailed software enabled clinical model leveraging pharmacotherapy, nutrition therapy, health coaching and remote physiological monitoring to support patients with obesity and other metabolic conditions to achieve their weight loss and wellness goals. - This role can be part-time or full-time. BACKGROUND AND EXPERIENCE - The ideal candidate will be a board certified Nurse Practitioner with at least 2-3 years of experience in bariatric medicine, endocrinology, primary care and/or related fields - Certification in obesity medicine a plus - Must have experience with using anti-obesity pharmacotherapy - Active, unrestricted license to practice medicine in New York or California with additional state licenses a plus. - Demonstrated excellent written/verbal communication skills. - Competency in the genetic, biologic, environmental, social, and behavioral factors that contribute to obesity and a thorough understanding of the treatment of obesity. - Competence with non-surgical therapeutic interventions including diet, physical activity, behavioral change, and pharmacotherapy, and in providing peri- and post-surgical care of endoscopic, metabolic and bariatric surgery patients ADDITIONAL DETAILS: - Market-based compensation commensurate with experience. - Malpractice coverage will be provided - Flexibility to deliver care at your convenience - Quality initiatives that guide the highest standards of evidence-based, compassionate care IDEAL QUALITIES: - A non-stigmatizing, empathetic demeanor and virtual “bedside” manner. - Excellent at collaborating and forming respectful relationships with colleagues regardless of function or level of seniority. - Enthusiasm for innovation in healthcare and leveraging software to improve patient outcomes. - Creative and flexible, but always puts the patient first - You will need superior communication skills and excellent technical abilities. You must be comfortable interacting with patients over telehealth communication. WHAT TO EXPECT AT ACCOMPLISH HEALTH: - We are a remote-first, progressive, and technology focused workplace - We are a mission-driven organization made up of veteran entrepreneurs and healthcare professionals passionate about treating obesity and related metabolic conditions. - We care about the well being and growth of our patients, employees, and community. - We are an equal opportunity employer that values diversity at our company. - We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status - We are backed by top venture capitalists and entrepreneurs who have invested in or founded billion dollar startups

Remote Neurologist IONM Reader Make us your new Home. Help us accelerate the growth of our expanding medical services private practice. Neuro Alert is seeking board certified Neurologists with relevant clinical experience to join its organization on a contracted basis to perform remote Neurological Intra-operative Monitoring (NIOM). Founded in New York by a neurologist, Neuro Alert is a leader in the field of NIOM. The organization’s foundation is based on care, education, partnership, collaboration, and innovation. They are known for longstanding interpersonal relationships, for an overall commitment to its patients and clients, and for handling complex trauma procedures and other cutting-edge monitoring practices. This is an amazing opportunity to join an industry leader, collaborate with physician peers within the organization, and provide remote oversight from the comfort of your home office. You will lead by example and foster an environment of excellence through personal development and professional growth. We are particularly interested in forming future relationships with like-minded Neurologists who share a collegial vision of building our group practice model and collaborating by working closely together on casework, teaching, and educational projects. OVERVIEW OF JOB FUNCTION AND DUTIES: - Remotely monitor IONM procedures in adult and pediatric patients. - Monitor daytime and night/weekend cases during regular participation in a call schedule. LOCATION: - Anywhere in the United States (preference in Eastern or Central time zone). SKILLS, KNOWLEDGE AND ABILITIES: - A commitment to clinical excellence is required. - An interest in education and participating in research work involving ongoing patient outcomes. - Desires for a long-term commitment with the team of clinicians in a mutually fulfilling professional relationship. EDUCATION, EXPERIENCE, AND LICENSE REQUIREMENTS: - A minimum of 1 year of remote IOM oversight required. - 2 or more years are preferred. - Board certification in neurology is required. - Experience in NIOM is required. - Experience in peripheral nerve, muscle disease, seizures, vascular cases, and neuro-intensive care is preferred. - Fellowship in NIOM or Board Certification in Clinical Neurophysiology, Peripheral Nerve or Epilepsy is also preferred. - Publications showing an interest in research and teaching are preferred. - Licenses in NY, NJ, CT, TX, LA, CO, IN preferred but not required. COMPENSATION: - The compensation structure focuses on an independent contractor model. - Individual cases, as well as time on call, are compensated. - Neurologists who have a private practice and/or academic practice work well with our compensation model. SOFT SKILLS: - Possess positive and highly communicative interpersonal skills. - Team-oriented. - Look to contribute to the company’s growth. WORKING CONDITIONS: - Must have a designated work area at home that has sufficient space to accommodate equipment to perform the job responsibilities, that has full and uninterrupted access to the internet, and that provides a quiet, professional, secure, and confidential work environment. - Must have the ability to provide undivided attention to IONM on days scheduled to work. HOW TO APPLY: - Please include a cover letter and CV. IMPORTANT: Principals only. Recruiters – please do not contact this job poster. Neuro Alert is an Equal Opportunity Employer. Employment with Neuro Alert is at-will.

Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebia we take that number very seriously and every day we come to work, with the purpose of bettering the lives of each person impacted by kidney disease and the renal community that serves them. Our tenacious, passionate employees’ challenge the status quo and work to develop unique therapeutics that have the potential to set new standards of care for people living with kidney disease. This is life-changing work, and we are all in, are you? Job Summary Reports To: Director, Field Medical Team Location: CA (Northern) As a field-based medical expert, the Senior Medical Science Liaison supports Akebia’s products and therapeutic areas by advancing scientific and collaborative relationships and acting as a conduit for timely translation and communication of knowledge with key members of external healthcare communities and internal stakeholders towards optimized patient outcomes. The MSL function is anchored in educating external and internal stakeholders in the science behind, and safe and appropriate use of our products. The MSL will gather and translate relevant and actionable insights from their external interactions and provide Medical Leaders with information that identifies scientific and educational gaps. The MSL supports the generation of clinical-scientific knowledge and applies subject matter expertise and experience to special projects. Essential Functions & Duties - Acquire and maintain an advanced level of clinical-scientific knowledge in the anemia and CKD landscape and other disease states(s) related to Akebia’s products. Maintain a basic level of clinical-scientific knowledge about the broader portfolio of Akebia’s products and the diseases they treat. - Identify and engage appropriate Key Opinion Leaders (KOLs) or Key Medical Experts (KMEs) and Healthcare Professionals (HCPs) within the renal/nephrology space in objective-based interactions with which to develop professional relationships and exchange clinical-scientific information relevant to Akebia’s products and areas of therapeutic interest. - Accurately and compliantly interpret and disseminate balanced and factual scientific, clinical, and health economic data. Gather and evaluate new information as it applies to Akebia’s products and areas of therapeutic interest. - Gather, translate, and communicate actionable, strategy-aligned insights from scientific, educational, and conference setting interactions. - Respond to unsolicited requests regarding any Investigator Sponsored Study (ISS) within the ISS program. Support ISS submissions through internal review and approval processes. Monitor and communicate progress for those ISSs approved and supported. - Deliver approved educational programs to relevant healthcare audiences (e.g. HCPs, Managed Care Organizations, Dialysis Organizations (DOs), Specialty Pharmacies, etc.). - Collaborate with Akebia’s clinical team to coordinate and optimize educational and research support for sites/investigators participating in Akebia’s clinical trials. - Identify educational needs within the medical community around anemia in CKD management. - Adhere to all regulatory and compliance guidelines and company policies in all aspects of scientific dissemination of information, including responses to unsolicited requests for medical information. - Attend scientific and medical meetings. Skills & Experience Basic Qualifications - Advanced clinical or medical degree (MD, PharmD, PhD, NP, PA or equivalent). - 3+ years of MSL experience in the renal/nephrology space required. - Strong clinical and pharmaceutical background with CKD/nephrology required. - Strong verbal and written communication and presentation skills. - Excellent organizational skills. - Excellent strategic thinking, negotiation abilities, and problem-solving. - Ability to work independently as well as cross functionally. - Demonstrated ability to independently work under pressure in a compliant and highly. regulated environment. - Travel 50-60% Preferred Qualifications - Advanced knowledge and experience within the Dialysis Organizations (DOs) Compensation: Targeted Base: $169,875 - 209,846 *Base Compensation for this role will depend on a number of factors including a candidate’s qualifications, skills, competencies, and experience, and may fall outside of the range shown. Base pay is only one component of the company’s total rewards package, all regular employees are also eligible for the corporate bonus program or the incentive compensation program (if applicable), as well as equity. Additional benefits include health care, vision, dental, retirement, PTO, etc. Are you an Akebian? An Akebian is curious, empathetic, and values making connections to people and ideas. Akebian’s aren’t afraid of diving in and owning a process or a problem, because we all want to deliver a great solution. Akebian’s believe that we are better together because we are all working toward a common purpose – to better the life of each person impacted by kidney disease. Want to learn more about what it means to be an Akebian? Visit our website: www.akebia.com