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Canon USA & Affiliates

Mgr Medical Affairs - Clinical Scientist Sr

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What they do

A Clinical Supervisor or Manager supervises staff and manages services in a clinical program. May provide clinical supervision for nursing, counseling or home health care staff. Works to ensure quality patient care. Trains and develops clinical staff and manages clinical program budgets.

$105,990 / year median in the U.S.

+8% projected growth

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Job Description

Mgr Medical Affairs - Clinical Scientist Sr - req1770 OVERVIEW Work as part of a dynamic and fast-paced team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment. Generate scientific and clinical evidence via product evaluations and research in order to highlight advantages of the technology while maintaining alignment with the business strategy. Participate as a technical expert of the product line technology and communicate product intelligence to internal teams, key partners, collaborators, and external experts. Effectively interact with multiple teams including R D, global and local business, marketing solutions, regulatory, applications, and service. Manage key clinical customer/partner relationships in order to comprehensively support Canons business objectives while serving the needs of patients.
RESPONSIBILITIES
+ This is a remote position + Clinical research and validation. Manage collaborative research and clinical evaluation projects at collaboration/partner sites including data collection, protocol development, data acquisition, phantom studies, equipment evaluations, post processing, co-writing papers, IP and technology transfer support, and development of presentations. + Provide evidence-based guidance on scientific and clinical requirements for new products and features to meet market needs. + Support regulatory activities providing technical/market expertise, and reviewing study/test-plan design. Influence regulatory specifications and claims strategy by providing scientific and clinical consultation during early phase development. + Work with Strategic Development team to evaluate product claims and specifications — including testing of default protocols to ensure acceptance by industry standards (e.g., The Joint Commission and ACR ). Communicate relevant evaluation results via appropriate channels to internal and global research teams. + Support, design, and execute internal and external product evaluations. 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 regula To view full details and how to apply, please login or create a Job Seeker account