Collecting information
Organizing data
Minimum 10 years of successful medical device, healthcare technology, or healthcare services sales experience. Our diverse backgrounds across healthcare, medical device, technology, software, data science, and operations enable us to solve complex clinical challenges with rigor and creativity. The N
You’ll build trusted relationships with clinical teams and purchasing departments while driving sales of high-quality medical equipment. Whether you come from a clinical background or a B2B sales environment, if you’re ready to make a difference—you’re exactly who we need. Solutions Consulta
Multi-location healthcare billing experience. Medical Billing Specialist (Revenue Cycle Management) – Bilingual Spanish Preferred. Medical Billing Specialist with demonstrated.
Compliance & Quality Assurance Engineer. Develop, review and accept Quality Assurance Plans (SQAP/HPAP) to ensure certification compliance. Understand, update, and maintain QMS systems in compliance with ISO9001, AS91000, and other equivalent industry standards in addition to ensuring compliance to
The Clinical Sales Representative (CSR) will report to the Clinical Sales Manager with primary responsibility for delivering an excellent customer experience for all Galaxy customers within their territory. Our Clinical Sales Team is a dynamic and collaborative group committed to revolutionizing the
Candidates without both healthcare industry sales and software/SaaS sales backgrounds will not be considered. Minimum 2 years of healthcare industry sales experience. Familiarity with PACS, RIS, medical imaging, or clinical IT workflows.
Apply knowledge of clinical research to provide recommendations and direction to clinical research teams to ensure budgetary compliance throughout all phases of the Clinical Trial Financials Lifecycle. The Clinical Trial Budget Specialist II will coordinate the day-to-day study-related activities of
Organize study participant charts and files, and distribute to appropriate locationCollect required data from study coordinators and research nurses, and enter onto clinical research forms and into computerized databaseVerify accuracy of bills and stipendsGenerate letters to be sent to study partici
This role is responsible for strengthening clinical standardization, regulatory compliance, documentation integrity, quality improvement, and vaccine program oversight to support Novir's continued growth and operational excellence. Experience in healthcare quality, compliance, clinical operations, e
The Research Regulatory Specialist is responsible for gathering regulatory documents and preparing IRB applications, amendments, and continuing review submissions for human subject research, ensuring compliance with Federal, State, and Institutional Standard Operating Procedures. Collaborate with Re
Required Qualifications Bachelor's degree from an accredited university or college OR high school diploma/equivalency degree plus 6+ years of clinical or quality experience 2+ years of quality or clinical experience Desired Characteristics Strong oral and written communication skills. Job Descri
Clinical Research Trials Program Administrator. Perform the day-to-day administrative activities of the clinical research trials program. Assure compliance with all relevant IRB and other regulatory agency requirements.
Assure compliance with all relevant IRB and other regulatory agency requirements. Perform the day-to-day administrative activities of clinical research trial programs. The Medical College of Wisconsin (MCW) is an Equal Opportunity Employer.
Summary Assist study coordinators by providing administrative and data collection support for clinical research studies. Code and enter onto clinical research forms and into computerized database. Primary Responsibilities Under direction of the study coordinator or principal investigator, conduct r
We are seeking a Regulatory & Quality Assurance Specialist to join our team!. Regulatory & Quality Assurance Specialist. DME by maintaining regulatory and compliance processes, documentation, and records in alignment with applicable federal, state, internal, and quality requirements.
The Medical College of Wisconsin seeks a dedicated individual to assist study coordinators by providing vital administrative and data collection support for clinical research studies. The role involves conducting research activities, coordinating patient visits, and managing study documents while en
A research institution in Milwaukee is seeking an Administrative Support professional for clinical research studies. Ideal candidates will possess a solid knowledge of biology and chemistry, strong problem-solving, and writing skills.