• Serves as the medical monitor for clinical trials and assists in resolving major issues that may affect their assigned studies. • Partners with the Clinical Scientist, Data Manager, Pharmacovigilance Scientist, and other members of the study team to conduct the clinical studies, including study design, operational feasibility assessment, and site selection. • Provides expert opinion and review for creation of key study documents, including clinical study protocols, safety and medical monitoring plans, charters, and informed consent forms. • Interacts closely with Regulatory Affairs to contribute or review clinically relevant components of investigator brochures, briefing books, and other regulatory documents and communications. • Conducts investigator meetings, leads site initiation visits, and maintains relationships with clinical trial investigators. • Works with internal discovery and translational scientists, technical operations/manufacturing teams, regulatory affairs, safety and pharmacovigilance, and external consultants or CROs in a cross-functional manner. • Oversees and supports the gathering, analyzing, reviewing, interpreting, and reporting of clinical safety and efficacy data. • Supports publication and external communication strategy, acting as owner of clinical data, collaborating in the creation of meeting abstracts, presentations, and publications, and presenting at investigator meetings and scientific conferences as required.

Role Description We are seeking an experienced Physician (MD or DO) passionate about remote care delivery. In this role, you will support diabetes education and management by conducting phone visits for initial member consultations. You will be responsible for: - Evaluating diagnoses, medications, and lab results to assess member acuity and validate candidacy for our clinical program. - Providing call-based care to members in Perry Health's Remote Patient Monitoring (RPM) program. - Delivering swift, empathic care to members and assessing their clinical competencies. - Evaluating medical history and data to determine member eligibility for the clinical program. - Serving as a primary clinical point of contact for practice-wide escalations. - Collaborating with the broader care team — including RNs, RDs, and Accountability Coaches — to reinforce clinical goals and SMART goal progression. - Adhering to Perry Health policies, procedures, and standard operating procedures to ensure ongoing clinical quality and compliance. Qualifications - Medical Degree (MD or DO) from an accredited institution. - Valid, unencumbered state medical license required. - Multi-state licensure required — must hold active licensure in at least 3 of the following states: AL, GA, IL, IN, LA, MS, NC, OH, TN. - Minimum 3+ years of experience managing patients with diabetes. - Familiarity with continuous glucose monitors (CGMs) and behavior change theory is a plus. - Motivated learner, willing to acquire proficiency with the necessary technology (computers, software applications, phone systems); experience or training in Motivational Interviewing to support sustainable behavior change is a plus. - Creative thinking, an eye for detail, ability to work independently, a positive attitude, and the ability to excel in a fast-paced atmosphere while collaborating with diverse groups at all levels of the organization. - Spanish-speaking highly preferred. Requirements - Candidate must hold valid, unencumbered medical licensure in at least 3 of the following states: AL, GA, IL, IN, LA, MS, NC, OH, TN. - 1099 flexibility; you set your own hours with at least 10 hours of weekly availability. - Provide availability for the next two months by the 15th of each month. - Must reside in the United States with consistent access to a clean, quiet workspace; solid internet connection; and proficient technical experience. Compensation & Payment Terms - Contractors are paid on a monthly basis following Net 30 payment terms. - Clinical Pay: $40.00 per completed consult. - Consults are scheduled in 20-minute slots and require a minimum of 15 minutes of engagement time per member — inclusive of live conversation, chart review, and care coordination — for the visit to be billable. - Non-Clinical Pay: $30.00/hour flat rate for required meetings and training. - Example: Completing three consults within an hour pays a total of $120 for that hour.

Leader Medical Affairs - req1704 Location: This is a remote-based position in the USA Job Description: OVERVIEW Lead a team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment. Manage clinical evidence generation strategy and implementation through clinical research and evaluation activities. Identify and build key clinical customer/partner relationships in order to comprehensively support clinical evaluation plans and product messaging strategies while serving the needs of patients. Represent Canon medical as a clinical and technical expert of the product line technology and communicate product intelligence to company stakeholders, key partners, collaborators, and external experts. Effectively collaborate with multiple teams including R&D, global and local business, marketing solutions, regulatory, applications, and service. RESPONSIBILITIES This is a remote based position in the USA - Manage clinical research and validation strategy for the product-line. Lead a team of clinical researchers to achieve clinical research and validation objectives including hypothesis-driven research and clinical evaluation projects at luminary institutions. - Provide evidence-based guidance on scientific and clinical requirements for new products and features to meet market needs. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team. - Develop clinical product messaging and support Solutions Marketing to develop a go-to-market story. - Represent Canon as a spokesperson for product line technology at educational and scientific industry events. - Support regulatory activities by overseeing image quality review with external medical experts, providing technical/market expertise, and consulting on study/test-plan design. Influence regulatory strategy by providing scientific and clinical consultation during early phase development. - Work with Strategic Development team to evaluate product claims and specifications. Provide relevant evaluation results via appropriate channels to global business team. - Develop and execute clinical evaluation strategy for emerging products and features. Explore expansion of clinical use. Provide product validation results and communicate scientific and clinical benefits to company stakeholders such as Solutions Marketing for the purposes of product collateral development. - Support Solutions Marketing in developing collaterals. Provide relevant scientific and clinical data, review collaterals for scientific accuracy, and work jointly with regulatory to ensure adherence to clinical claims and technical specifications. Support Solutions Marketing on the development of scientific and clinical arguments for products and counter-arguments against competition. - Support education teams in development of videos and training programs by providing clinical and technical expertise and evidence. - Support Clinical Collaborations in Medical Advisory Board (MAB) activities related to the product line. - Support Clinical Collaborations by actively participating in hypothesis-based research grant proposal review committees for all product lines. - Work with Clinical Collaborations database administrator to ensure research activities are kept to schedule and recorded on a regular basis. - Participate in BU and Medical Affairs meetings and provide clinical and technical expertise to support business decisions. - Provide clinical, technical, and product education to enhance the knowledge base of the Market Development, Solutions Marketing and Applications teams. - Collaborate with healthcare economics personnel to translate economic benefits of clinical research programs for the benefit of marketing and sales programs. - Communicate known clinical or technical product issues via appropriate channels. Work with relevant team(s) (e.g., Strategic Development, Regulatory, and Service) to quickly implement market accepted solutions. - Represent Canon in industry organizational activities (e.g., MITA, IEC, AAPM, RSNA, ISMRM, ACR, ABR, QIBA, etc.). QUALIFICATIONS - Strong communication skills, including credible interaction with prominent academicians and demonstrated skill at scientific writing and presenting. - Proven ability to operate effectively in a matrix organizational structure. - Detailed clinical and technical knowledge of CT, MR, X-ray, Ultrasound, or Vascular systems. - Proficiency with computers in windows-based software environment. - Prefer experience with managing dynamic teams of individuals with diverse skills and expertise. - PhD preferred - Other PhD and/or MD medical imaging physics, engineering, or one of the clinical sciences. - 10 years' experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Pay Information: Min $132,000 to Max $213,00 annual equivalency #LI-Remote About us! Canon Medical Systems USA, Inc., a world leader in diagnostic imaging, is in search of qualified candidates to fill our open positions. Canon Medical Systems offers a competitive salary and benefits package, we support a diverse workplace and are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, sex, color, sexual orientation, gender identity, religion, national origin, protected veteran status, or on the basis of disability. We invite you to join and become part of our Canon family.

• Participate in the design and execution of clinical studies in a new therapeutic area (Gastroenterology) • Contribute clinical and strategic perspective to EoE development program through BLA • Serve as a medical monitor, working closely with the CRO, clinical operations, and pharmacovigilance on study execution, including but not limited to safety reporting, point of escalation for medical monitoring matters, development and execution of the Medical Monitoring Plan • Contribute to the design of trials, and develop protocols and other relevant documents for individual studies • Lead study start-up activities • Direct day-to-day clinical and medical execution of studies • Work closely with cross-functional colleagues, including, but not limited to, clinical operations, regulatory, biostatistics, and data management, to ensure timely and flawless execution of clinical plan • Partner with clinical operations on site selection, recruitment, and CRO management • Partner with medical affairs to build and maintain strong relationships with PIs, including support of Advisory and Scientific Boards and Investigator Meetings • Serve as primary medical point of contact for sites and PIs for the assigned study, as applicable