Role Description The Medical Education Lead (MEL) will support the delivery and embedding of medical education in North America in order to develop the clinical skills, knowledge, confidence, and competencies of the internal team and the health care professional’s community with the aim of increasing therapy awareness & adoption. The MEL will be a business partner who will engage in identifying and overcoming unmet medical needs especially related to apheresis and related cell therapies. The MEL will act both internally and externally to develop therapy adoption programs together with NA thought leaders and prescribers. The MEL may be called on to support, participate and/or drive special projects, such as internal and external education and medical congresses. The MEL will respond to medical, scientific & clinical information requests with regards to high-level troubleshooting and procedure optimization. Duties and Responsibilities - Develops and maintains professional scientific relationships in areas critical to TerumoBCT with thought leaders and health care professionals in key medical or blood centers, with medical professional associations and patient advocacy groups. - Works with the sales and marketing team to build knowledge, confidence, and competence to drive clinical excellence and help to achieve unmet medical needs in the field of Apheresis. - Serves as a primary Medical Affairs contact involved with clinical/scientific information exchanges. - Identifies opportunities and conducts formal presentations to essential groups as requested by medical and technical healthcare professionals. - Maintains expert knowledge and understanding of clinical, scientific, and technical information in areas critical to Terumo BCT. - Supports the commercialization team and global product marketing where appropriate, providing input as needed in product innovation and unmet medical needs. - Active participation in developing tools and resources, e.g., training material. - Attends & provides coverage at national & regional medical education venues and brings back medical insights to key internal stakeholders for accurate planning. - Responds to and tracks medical information requests from healthcare professionals and decision makers. - May lead and/or coordinate special projects as it relates to building scientific & medical competencies within the organization. Qualifications - Registered Nurse (RN) credentials required. - Master’s Degree or Bachelor’s Degree strongly preferred. - Minimum 6+ years’ experience in apheresis, blood product management, blood transfusion, or blood banking. - Professional up-to-date credentials and/or certifications are preferred: i.e., Certification in Apheresis. - Apheresis technology experience is strongly preferred. - Previous experience with genetic hematological disorders such as sickle cell disease will be a plus. - Strong interpersonal, influencing, and negotiation skills with different types of internal and external stakeholders. - Team player, patient and customer-focused, problem solver with clear focus on end-results. - Ability to work autonomously and independently with time management skills to effectively manage field-based responsibilities. - Ability to work in a matrix structure, i.e., maintains strong working relationships with various other departments. - Excellent in written and oral communication skills in English. Any additional language will be a plus. - Naturally outgoing and relationship-oriented, able to build trust and credibility with healthcare professionals, internal experts, and cross-functional partners. Requirements - Location: Lakewood, Colorado or Remote. - Typical Office Environment requirements include: reading, speaking, hearing, close vision, walking, bending, sitting, and occasional lifting up to 20 pounds. - Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties. Benefits - Competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs. - Multiple group medical, dental and vision plans. - A robust wellness program. - Life insurance and disability coverages. - A variety of voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance, and much more. - 401(k) plan with a matching contribution. - Vacation and sick time programs for associates.

• Performs concurrent analytical reviews of clinical and coding data to improve physician documentation for all conditions and treatments from point of entry to discharge. • Ensures an accurate reflection of the patient condition in the associated Diagnosis Related Group (DRG) assignments, case-mix index, severity of illness (SOI), and risk of mortality (ROM) profiling, and reimbursement. • Facilitates the resolution of queries and educates members of the patient care team regarding documentation guidelines. • Collaborates with coding professionals to ensure accuracy of diagnostic and procedural data and completeness of supporting documentation.

• Author clinical study reports (CSRs), protocols, informed consent forms (ICFs), narratives, investigator brochures, and other regulatory documents across therapeutic areas • Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines • Identify the right parties for content decisions and synthesise discussions into clear, accurate prose • Review work of junior or outsourced writers and CSR-related documents like Statistical Analysis Plans and TFLs • Write plain-language content such as ICFs and explain complex medical concepts to lay audiences • Adhere to applicable guidelines, templates, SOPs, and internal training while contributing to process improvement across Medical Writing and Global Development • Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict

• Implements all activities related to the preparation of defined medical and regulatory documents • Supports documents for regulatory submissions to US and global health authorities • Collaborates with cross-functional team members to ensure accurate and timely completion and delivery of high-quality documents • Supports clinical trial transparency and disclosures • Contributes to departmental development through editorial and review support for document templates