Job Description Agent(e) de liaison médicale et scientifique national - Ophtalmologie Territoire: Canada Relevant du Responsable des Liaisons Médicales et Scientifiques, Médecine générale et spécialisées, l’agent(e) de liaison médicale et scientifique national est un professionnel médical sur le terrain dont la responsabilité principale consiste à communiquer d’égal à égal de façon non promotionnelle et à utiliser son savoir-faire social poussé pour offrir des renseignements médicaux et scientifiques aux leaders scientifiques ou les décideurs clés basés sur un échange et des services scientifiques de pointe favorisant les intérêts et les besoins professionnels du partenaire professionnel. L’agent(e) de liaison médicale et scientifique s’assure qu’il ou elle connaît à fond le domaine thérapeutique (ophtalmologie) et toutes les études importantes tant en cours que terminées, les renseignements sur les produits concernant les thérapies pertinentes de Notre entreprise et autres sociétés, les données cliniques et les données sur les produits en développement pertinentes pour offrir les données les plus équilibrées aux les leaders scientifiques, aux décideurs clés et au secteur de la santé pour améliorer les soins aux patients. Rôles et responsabilités: - Faire des échanges non promotionnels d’égal à égal de renseignements médicaux et scientifiques avec les leaders scientifiques ou les décideurs clés dans la mesure où la loi et la réglementation locales, les codes sectoriels locaux et les autres dispositions du mode opératoire normalisé médical sur le terrain le permettent. - Obtenir des intuitions profondes sur les maladies, le domaine thérapeutique et les besoins en matière de soins de santé, les lacunes dans les données et les défis liés à la géographie locale. - Représentant les Affaires médicales à des événements médicaux locaux ou régionaux non promotionnels (p. ex., congrès ou symposiums médicaux), collaborer à la coordination des renseignements scientifiques avant l’événement et aux résumés scientifiques après l’événement. - Répondre aux demandes non sollicitées de renseignements médicaux ou scientifiques ou sur les produits en développement ou sur le marché ou aux indications des leaders scientifiques ou les décideurs clés au moyen de matériel scientifique approprié et approuvé. - Répondre (seul à seul) aux demandes non sollicitées de renseignements sur les recherches de la société et/ou les activités en matière de subventions en aiguillant les leaders scientifiques ou les décideurs clés vers les ressources appropriées de la société pour les subventions, la participation à des essais cliniques commanditée, le programme d’études de chercheurs de Notre entreprise et les recherches sur les résultats. - Participer aux réunions du conseil consultatif scientifique ou aux forums de discussions d’experts quand il y a un rôle défini. - Participer aux plans des Affaires médicales et à la mise en œuvre d’activités indiquées dans les plans des Affaires médicales. - À la demande des Opérations mondiales liées aux essais cliniques ou du Centre mondial d’études d’observation et d’études de vie réelle, appuyer l’identification d’investigateurs de l’étude potentiels pour l’étude commanditée. Qualifications: - ​Détenir un diplôme en pharmacie (BSc.) ou doctorat (Pharm. D.); doctorat (PhD) en sciences de la santé (lié au domaine de la maladie de préférence) ou en médecine (MD). - Minimum de deux ans d’expérience comme agent(e) de liaison médical en industrie - Connaissance du domaine thérapeutique de l'ophtalmologie (documentation de base et clinique) est un atout. - Capacité démontrée à acquérir et à entretenir des connaissances sur les produits, les maladies et les compétiteurs. - Compétences linguistiques : la maîtrise du français est requise - Solides compétences en relations interpersonnelles. - Compétences en gestion des budgets. - Très bonne connaissance des politiques et des procédures de la société ainsi que des normes, lois et règlements de l’industrie. - Capacité à analyser et à comprendre la communauté locale de la pratique. - Capacité à comprendre et à assimiler des concepts scientifiques complexes - Connaissance avancée de la technologie et des logiciels Office. - Compétences avancées en analyse, en planification, en mise en œuvre et en suivi. - Compétences avancées en négociation, en présentation et en animation. - Compétences avancées en gestion de projet. - Le (la) candidat(e) doit être basé(e) au Québec ou en Ontario Nous sommes fiers d'être une entreprise qui embrasse la valeur de rassembler des personnes diversifiées, talentueuses et engagées. La façon la plus rapide d’innover est de rassembler des gens de diverses opinions dans un environnement inclusif. Nous encourageons nos collègues à remettre en question avec respect les problèmes de réflexion et d’approche de l’un et de l’autre. Nous sommes un employeur souscrivant au principe de l’égalité d’accès à l’emploi et nous sommes déterminés à favoriser un milieu de travail inclusif et diversifié. Required Skills: Adaptability, Clinical Data, Data Analysis, Interpersonal Relationships, Medical Affairs, Medical Marketing Strategy, Ophthalmology, Project Management, Relationship Building, Scientific Communications, Scientific Exchange, Scientific Leadership, Teamwork, Therapeutic Knowledge Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Secondary Language(s) Job Description: National Medical Scientific Liaison - Ophthalmology Territory: Canada Reporting to the Medical Scientific Liaison Manager, General and Specialty Medicine, the National Medical & Scientific Liaison is a field-based medical professional whose primary responsibility is to engage in non-promotional peer-to-peer communication, using very strong interpersonal skills & provide medical/scientific information to Scientific Leaders and Key Decision Makers based on cutting-edge scientific exchange and services oriented towards the stakeholder’s professional interests & needs. The Medical Scientific Liaison is responsible for ensuring that they are fully versed in the therapeutic area (Ophthalmology) and up to date on all major studies, both ongoing and completed, product information on our Company’s and other companies’ relevant therapies, clinical data and relevant pipeline data to provide the most balanced data to Scientific Leaders, Key Decision Makers and the healthcare community to improve patient care. Roles and responsibilities: - ​Engaging in non-promotional peer-to-peer exchange of medical and scientific information with Scientific Leaders or Key Decision Makers to the extent permitted by law and local regulation, local industry codes, and other provisions of the Field medical standard operating procedure. - Gaining deep insights on disease, therapeutic area and healthcare needs, data gaps and challenges in their local geography. - Representing Medical Affairs at local or regional non-promotional Medical events (e.g. Medical Congresses and Symposia) They may collaborate in the coordination of pre-event scientific information and post-event scientific summaries. - Responding to unsolicited requests for medical, scientific, pipeline or marketed product information or indications from Scientific Leaders or Key Decision Makers utilizing appropriate approved scientific materials. - Responding (one-to-one) to unsolicited requests for information on company research and/or grant activities by directing Scientific Leaders or Key Decision Makers to appropriate company resources for grants, sponsored clinical trial involvement, our Company’s Investigator Study Program, and outcomes research. - Participating in Scientific Advisory Board Meetings or Expert Input Forums when there is a defined role. - Participating in the development of Medical Affairs Plans and implementation of activities identified in the Medical Affairs Plans. - At Global Clinical Trials Organization, or Center for Observational and Real World Research personnel request, supporting the identification of potential study investigators for sponsored study Qualifications: - Hold a degree in pharmacy (Bachelor's degree or Doctorate); PhD Degree in Health Sciences (preferably in related disease area) or Doctorate in Medicine. - Minimum of two years of experience as Medical Scientific Liaison - Knowledge in the therapeutic area of Ophthalmology (both basic and clinical literature) is an asset. - Demonstrated ability to acquire and maintain product, disease and competition knowledge. - Language: Fluency in French is required - Strong interpersonal skills. - Budget management skills. - Strong knowledge of Company policies, procedures, industry standards, as well as laws and regulations. - Ability to analyze and understand local community of practice. - Ability to comprehend and integrate complex scientific concepts - Advanced knowledge of Office technology and related software. - Advanced Analysis, Planning, Implementation and Control skills. - Advanced negotiation, presentation, and facilitation skills. - Advanced project management skills. - Candidates must be based in Ontario or Quebec We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 50% Flexible Work Arrangements: Remote Shift: Not Indicated Valid Driving License: Yes Hazardous Material(s): no Job Posting End Date: 04/15/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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.