GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: The Medical Science Liaison (MSL) is a field-based scientific expert responsible for engaging with Key Opinion Leaders (KOLs), healthcare professionals, and medical practices to deliver evidence-based insights about the company’s products and the latest scientific advancements. The MSL plays a pivotal role in translating clinical research into practical, real-world applications, ensuring that scientific knowledge is effectively communicated and utilized. In this role, the MSL actively contributes to educational programs, gathers valuable real-time insights from healthcare professionals (HCPs), and provides critical support to both internal and external stakeholders. Key responsibilities include representing the company at regional and national conferences, facilitating compliant scientific exchange, and engaging in appropriate off-label discussions with scientific peers, all while ensuring adherence to regulatory standards. This position is integral in bridging the gap between scientific innovation and clinical practice, driving informed decision-making within the medical community. MSLs at Tandem are also responsible for the following in a specific region: This role will cover the Central Region with our field team; Ohio Valley to Wisconsin down to Gulf Coast areas. - Develops and executes Medical Affairs education strategies for the Central Area, delivering scientific webinars, in-person presentations, and fostering peer-to-peer scientific exchange. - Partners closely with area-level commercial division leaders to engage healthcare professionals (HCPs) with peer-to-peer medical information exchange, relationship-building, and identification of appropriate fit for educational programs. - Arranges in person travel opportunities to deliver scientific presentations and develop relationships with HCPs. - Responds to both on-label and off-label inquiries from medical professionals on appropriate and safe device use and training, including virtual or in-person HCP consultations. - Supports medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, and review of promotional and educational materials. - Supports Market Access teams with clinical presentations on publications, and market trends to payers and regulatory bodies. - Provides ad-hoc educational webinars, presentations, or content to internal teams to support corporate initiatives (including scientific information, new indications for use, disease management, and device use). - Assists with set up and delivery of round tables with peer HCPs to elicit feedback. - Translates complex medical messages to enable clear and concise understanding by both external audiences and internal stakeholders. WHAT YOU’LL NEED: - MS, PhD, DNP, MD/DO, PharmD or equivalent combination of education and applicable job experience. - Clinical licensure (MD, RN, NP, etc.) preferred. - Certified Diabetes Care and Educator Specialist (CDCES), Board Certified in Advanced Diabetes Management (BC-ADM) or similar, preferred. - 3+ years of clinical diabetes, diabetes technology, or insulin pump industry experience. - Experience presenting or communicating scientific information to professional audiences. - Deep knowledge of diabetes disease state and clinical management of type 1 and type 2 diabetes, standards of care, and diabetes technology use in diverse populations. - Fundamental knowledge and/or experience with scientific and statistical analyses. - Professional experience interacting with patients, referral sources, and health care professionals. - Skilled at analytical problem solving and communicating with culturally diverse groups. Skilled in effective presentations of scientific data and materials. - Demonstrated knowledge of US FDA medical device regulations. - Understanding of international medical device regulations with specific knowledge of Canadian Medical Device Regulations and EU CE Mark may be relevant. - Excellent technical writing, editing, and proofreading skills. - Able and motivated to work independently and as a team member with many different departments. - Able to make and prioritize process and resource decisions based on overall team needs. - Ability to plan and execute clinical and regulatory preparation activities. - Skilled with MS Office applications as well as Adobe Acrobat. TRAVEL: Ability to travel by car or airplane (as well as overnights) independently up to 50% of the time and work a varied schedule to meet customer needs. Current negative Tuberculosis Skin Test and annual Tuberculosis screening with documented proof are required. WHEN & WHERE YOU’LL WORK: Remote: This position is remote and in the field, open to candidates within the United States. Equipment for the role will be provided and training will occur virtually. COMPENSATION & BENEFITS: The starting base pay range for this position is $136,000 - $160,000 annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package. Tandem offers health care benefits such as medical, dental, vision available your first day, as well as health savings accounts and flexible saving accounts. You’ll also receive 11 paid holidays per year, a minimum of 20 days of paid time off (with accrual starting on day 1) and you will have access to a 401k plan with company match as well as an Employee Stock Purchase plan. Learn more about Tandem’s benefits here! YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow. #LI-Remote #LI-DW1

• Provide medical and scientific leadership for Natera-sponsored oncology clinical trials focused on minimal residual disease (MRD). • Drive the design and execution of biomarker-driven interventional and randomized studies. • Serve as the program-level medical lead for Natera-sponsored MRD clinical trials across assigned oncology indications. • Define clinical development strategies and provide medical oversight across the full trial lifecycle. • Provide strategic and medical guidance to Clinical Scientists and act as Medical Monitor overseeing safety signal detection and risk mitigation. • Collaborate with cross-functional teams and partner with Regulatory Affairs to support submissions and responses.

Role Description The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Rheumatology in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization teams. They collaborate with our Research & Development Division's Early and Late Development functional areas, Value & Implementation Outcomes Research (VIOR), Policy, Commercial and Market Access to address opportunities in key countries. They engage with their network of scientific leaders and decision makers. This is a headquarters-based position in Our Company Research Laboratories Value & Implementation Global Medical and Scientific Affairs (Research & Development (R&D) VI GMSA). - Supports execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and regions. - Serves as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, Commercial, Publications). - Contributes to the development of a single global scientific communications platform. - Consolidates actionable medical insights from countries and regions. - Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about Our Company’s emerging science. - Organizes global expert input events (advisory boards and expert input forums) to answer Our Company’s questions about how to develop and implement new medicines or vaccines. - Aligns plans and activities with Global Human Health (commercial) executive directors. - Organizes global symposia and educational meetings. - Supports key countries with the development of local data generation study concepts and protocols. - Reviews Investigator-Initiated Study proposals from key countries prior to headquarters submission (ex-USA). - Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company medicines or vaccines. Qualifications - M.D., Ph.D. or Pharm.D. (M.D. preferred) and recognized medical expertise within rheumatology. - Minimum of 3 years experience in global/region medical affairs or clinical development. - Strong prioritization and decision-making skills. - Ability to effectively collaborate with partners across divisions in a matrix environment. - Excellent interpersonal, analytical, communication skills (written and oral) in addition to results-oriented project management skills. Requirements - At least 5 years Global medical affairs experience with proven track record of contribution to medical affairs strategies. - Customer expertise, especially of scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area. Benefits - Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family). - Retirement benefits, including 401(k). - Paid holidays, vacation, and compassionate and sick days.

MannKind Corporation (Nasdaq: MNKD) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions. With a focus on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, pulmonary fibrosis, nontuberculous mycobacterial (NTM) lung disease, and fluid overload associated with heart failure and chronic kidney disease. At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives. Position Summary The Medical Science Liaison acts as a highly experienced scientific expert and strategic partner within the Medical Affairs organization. This regional role is responsible for leading scientific engagement with key opinion leaders (KOLs) academic medical centers and healthcare professionals, driving advanced medical education initiatives, and providing strategic insights to shape clinical development and medical strategy. The (Senior) MSL also mentors and trains junior MSLs and leads initiatives that align with the medical affairs strategy, including education, research, congress planning, publications, and cross-functional collaboration. This role focuses on building strong scientific relationships, providing clinical and educational support, and ensuring the appropriate dissemination of medical and scientific information to advance evidence-based medicine and patient care. This is a field‑based role supporting the Southwestern Region (AZ, NV, UT, CA), with a primary focus on Southern California. The role requires up to 50% travel within the assigned territory. Key Responsibilities - Scientific Exchange & Education - Develop and maintain relationships with KOLs, HCPs, and academic institutions within regional territory - Provide balanced, scientific information on company products, disease states, and therapeutic areas. - Communicate with payors and formulary committees pre- and post-approval in accordance with FDA guidance, collaborating with market access and key account teams. - Strategic Leadership and Insights - Maintain expertise in disease states, emerging therapies, and healthcare trends to provide value to internal and external stakeholders. - Participate and/or lead project teams driving tactical activities aligned with medical affairs strategy. - Lead advisory boards and other strategic activities to inform medical and commercial directions. - Gather and communicate field insights to inform medical strategy and clinical development. - Identify emerging trends and unmet needs within the therapeutic landscape. - Stakeholder Engagement - Identify and engage key thought leaders and content experts across healthcare systems, payors, integrated delivery networks and other key accounts. - Cross-Functional Collaboration - Provide compliant scientific account support for commercial functions, including training for speakers. - Act as a scientific advisor to Clinical Research, Investor Relations, Business Development, and Corporate Communications. - Research & Data Generation - Identify and facilitate research opportunities aligned with company priorities, including collaborative and investigator-initiated studies and HEOR projects. - Collaborate with Clinical Research to support trial site identification and investigator engagement as needed. - Participate in medical writing for abstracts, publications, and scientific materials. Education and Experience Qualifications: • Education: - Advanced degree (Pharm.D., Ph.D., NP, PA, RN, MD, or equivalent) required. • Experience: - Experience in Medical Affairs or relevant therapeutic area and 3 - 5 years prior experience as an MSL preferred. - Deep understanding of clinical research, therapeutic area expertise, and ability to interpret scientific data. - Excellent communication, presentation, and relationship-building skills. - Ability to work independently in a field-based environment. - Proficient in Microsoft Word, Excel, Outlook, Teams and PowerPoint. • Industry Knowledge: - Deep understanding of the U.S. healthcare system and medical affairs. - Expertise with KOL engagement and stakeholder management skills. This role requires up to 50% travel and reports to the National Director, Field Medical Affairs and MSL Team Lead. #LI - Remote