In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
In this role, the selected candidate will lead and manage multiple research initiatives, developing innovative market positioning strategy that meets client requirements and industry standards and is skilled in content analysis, quantitative tracking, and qualitative assessment.
In this role, you will design and develop system wide solutions applying linear and integer math programming applications and integration with factory data systems to drive solutions to complex manufacturing problems. Identify and solve problems in factory performance.
This Clinical Research Coordinator is a full-time staff position in MWUs Institute for Healthcare Innovation (IHI). The general purpose of this position is to assist in execution of human and veterinary clinical research projects and studies under direction of the Associate Director of the IHI.
In this role, you will be responsible to work with a team of Programmers, DBAs and Architects in the Research Analytics group and will need to gain an understanding of the biomedical research domain to assist in the design, population and implementation of databases and project applications.
In this role, you will collaborate with members of the security, Risk, and global investigations teams to establish goals related to detecting, mitigating and taking action against malicious activity and actors.
This position is responsible for a high level of technical knowledge and application of that knowledge to department testing, clinical relevance, and complex problem solving skills. This position serves as a department resource, and is responsible for assisting with department compliance with all pertinent laboratory accrediting agency and regulatory requirements (e.g., CLIA 88, JCAHO, CAP, OSHA).
In this role, the selected candidate will perform tasks required by protocol, which may include obtaining patient medical history, systems review, phlebotomy, EKG, and cognitive assessment on patients. Collects vital signs. Maintains quality assurance on designated protocols. Collects data as required and assists in interpreting and evaluating results as required.
In this role, you must have experience in performing human factors and usability research: Defining studies, creating methods, refining methods; conducting studies; analyzing data; writing reports with recommendations.
The Staff Released Product Engineer is responsible for a wide variety of engineering work in support of medical devices including design changes, process/quality improvements and compliance issues. The Staff Released Product Engineer provides technical skills and team leadership, engaging internal and external capabilities as needed, coordinating and conducting technical studies which will lead to improved products & processes that meet specific businesses needs as well as regulatory requirements and quality standards.