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Be ready to walk through how you design or critique clinical questions, handle conflicting data, partner with R&D/marketing under compliance constraints, and manage priorities as a medical-affairs clinical scientist leader—not just as a pure lab scientist.
Strong fit if you combine clinical-science rigor with medical-affairs judgment, can lead evidence work for a large imaging/healthcare-adjacent manufacturer, and prefer on-site collaboration in the Springfield, Illinois area.
As Mgr Medical Affairs – Clinical Scientist at Canon USA & Affiliates, a typical day centers on clinical evidence for healthcare-related offerings: reviewing protocols and literature, coordinating with medical and commercial stakeholders, assessing safety and performance data, and translating findings into clear medical-affairs guidance for internal teams.
Build depth in clinical evidence, regulatory-aware medical writing, and stakeholder communication. Free options include Saylor Academy — Health Sciences courses (free) and Coursera — audit-track healthcare courses (free to learn).
The listing indicates on-site (remote = 0) in Springfield, Sangamon County, Illinois.
Manager-level medical affairs work with a clinical scientist focus—evidence, clinical insight, and cross-functional guidance rather than pure sales.
Saylor Academy Health Sciences courses are free; Coursera audit-track healthcare courses are free to learn.
Website: canonusaaffiliates.com
Public cache only — not an employee review.
The Mgr Medical Affairs - Clinical Scientist role at Canon USA & Affiliates is located in Springfield, Sangamon County and is a full‑time opportunity to generate clinical evidence that supports the adoption of advanced imaging technologies. About the Role In this position you will partner with clinical experts, product developers, and regulatory teams to design and execute studies that demonstrate the value of Canon’s imaging solutions in real‑world healthcare settings. What You'll Do Develop and manage clinical research protocols that evaluate product performance and safety. Coordinate with investigative sites to ensure timely enrollment, data collection, and quality oversight. Analyze study results and translate findings into scientific abstracts, manuscripts, and conference presentations. Collaborate with marketing and sales to create evidence‑based educational materials for healthcare professionals. Support regulatory submissions by providing clinical data packages and responding to agency inquiries. Maintain awareness of emerging clinical trends and competitor evidence to inform product strategy. Ensure all activities comply with Good Clinical Practice, institutional review board requirements, and company policies. What We're Looking For Advanced degree (PhD, PharmD, MD, or equivalent) in a life‑science or clinical discipline. Proven experience designing and executing clinical trials or real‑world evidence studies in the medical imaging or device sector. Strong grasp of statistical methods and proficiency with data analysis software (e.g., SAS, R, SPSS). Excellent scientific writing skills and a track record of peer‑reviewed publications or conference presentations. Ability to work cross‑functionally with R&D, marketing, regulatory, and commercial teams. Outstanding communication and presentation abilities for diverse audiences, including clinicians and executives. Familiarity with FDA, CE marking, and other relevant regulatory frameworks for medical devices. Based in or willing to relocate to the Springfield, Sangamon County area for on‑site work. About Canon USA & Affiliates Canon USA & Affiliates is a subsidiary of the global Canon Group, dedicated to delivering innovative imaging and healthcare technologies that improve patient outcomes. The organization fosters a collaborative environment where scientific rigor meets technical excellence to bring cutting‑edge solutions from concept to clinic. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform…
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