The Clinical Quality Assurance Specialist is responsible for providing a high level of expert support and feedback across various Departments; the CQAS role is also responsible for auditing, reporting and maintaining records of QA documentation.
A nursing leader responsible for providing expertise in the practice of nursing to produce quality outcomes, promote evidence based practice and demonstrate cost effective practices via collaboration with the patient, nursing personnel, physicians and all applicable stakeholders.
The Technical Application Specialist will serve as a subject matter expert for strategic product applications in Clinical Flow Cytometry; will take active part in system validation activities throughout all phases of product development process; providing voice of the customer expertise to marketing, business development, and product design teams; acting as a technical training and consulting resource for our in-house and field based technical teams, sales, and service organizations.
Provide product feedback to sales and marketing including customer feedback on product enhancements, service and policies through direct feedback as well as demonstration assessments and competitive developments.
Meets with existing and potential clients (e.g., physicians, physician office groups at hospitals) by traveling (in an automobile or airplane) to identify their clinical needs, goals, and constraints related to patient care and to discuss and demonstrate and train them on how company products can help them to achieve their goals.
The Clinical Sales Specialist is responsible for selling and account management activities for all products within the BioSciences Clinical Product Portfolio in hospitals and reference labs within their assigned territory.
The ideal candidate will have expertise in a broad-range of Clinical Flow Cytometry applications, including leukemia and lymphoma, immunodeficiency, cross-match, stem cell enumeration, DNA ploidy, transplant medicine, and antibody-mediated therapy assays.
In this role, the selected candidate will create and issue regulatory reports, including individual case safety reports using the submission Criteria; perform Source Verification quality checks as requested/necessary.