Job Location Smithfield, RI Smithfield, RI Position Type Full Time Education Level Bachelors Degree   Travel Percentage None Job Shift Daytime Job Category Professional / Experienced Description This position serves as a critical role for regulatory reporting, ensuring stakeholders make sound business decisions that directly impact Neighborhoods reportable metrics. Th

Duties WHAT IS LBI Large Business and International THE DIVISION? A description of the business units can be found at Vacancies will be filled in the following specialty areas Large Business and International Director Treaty and Trans Pric Ops Performs assignments based on breadth or depth of research and analyses involved in examinations that include complex issues cover

Duties WHAT IS THE OFFICE OF THE CHIEF PROCUREMENT OFFICER THE DIVISION? A description of the business units can be found at MAJOR DUTIES The following are the duties of this position at the full working level of GS 13 BU Negotiates settlements of disputes, proposals, and executes modifications. Requests changes or exceptions to federal procurement regulations. Prepares r

Under the general supervision of the Manager Purchasing Operations the Supply Chain Analyst is responsible for supporting system wide projects with accurate data and robust analyses. They will integrate an understanding of project goals with analytic expertise to assure and facilitate accurate data analysis. The Analyst will consult with Supply Chain users in the design d

Under the general supervision of the Administrative Manager (s) Research Projects Management ensures completion and performs a variety of functions related to the administrative aspects of research grants and contracts. Works with a variety of clients across all Lifespan affiliates. Responsibilities Collaborates with Administrative Manager (s) and Director in the developm

Reporting to the Lifespan Clinical Research Center Research Nurse Manager and in accordance with established departmental policies and procedures is responsible for representing the Lifespan Clinical Research Center to industry sponsors regarding the implementation operations and auditing of sponsored clinical research projects. The Sr. CRPC works collaboratively with the

Reporting directly to the Chief Development Officer of The Miriam Hospital and working in collaboration with the CDO development team hospital and volunteer leadership advances the fundraising program through successful stewardship. cultivation and solicitation of a donors managed in a major gift portfolio. Responsibilities Major Gift Officer Duties & Responsibilities Ide

Summary Reports to a departmental or divisional director and is responsible for direction of the research activities of a laboratory. Prepares writes and presents research papers. Provides consultation within area of expertise to individuals both internal and external to the hospital. Responsibilities Supervises postdoctoral fellows research assistants and other lab perso

Reports to a departmental or divisional director and is responsible for direction of the research activities of a laboratory. Prepares writes and presents research papers. Provides consultation within area of expertise to individuals both internal and external to the hospital. Responsibilities Supervises postdoctoral fellows research assistants and other lab personnel inc

Summary Reports to the Director of the Centers for Behavioral and Preventive Medicine. Research Scientists are responsible for direction of the research activities of a laboratory. They prepare and write grant proposals direct research supervise research staff members publish research papers in peer reviewed professional journals and provide consultation within area of ex

The Regulatory Assistant performs multiple tasks in order to meet compliance requirements in research. This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the department. The Regulatory Assistant supports the department and clinical

The Regulatory Assistant performs multiple tasks in order to meet compliance requirements in research. This position will be assisting in the overseeing of clinical research regulatory requirements for the department. The Regulatory Assistant will provide support in managing clinical trials for the department. The Regulatory Assistant supports the department and clinical

Summary Under the direct supervision of the Principal Investigator the Project Manager and Manager of Research Administration conduct specific research protocols associated with assigned research projects. All essential functions performed in this position reflect the age and culture specific needs of the participants. Responsibilities Assists in preparation of project pr

Under supervision and following established policies and procedures assists with review of electronic medical records (EMR) to extract protocol required data points for data entry and entering into protocol specific databases. Assist with organization and preparation of laboratory supplies required for clinical trials. Process research specimens as needed. Reviews literat

The Research Assistant will work with the Research Scientist and assist in coordinating various research studies. Job responsibility includes but is not limited to literature review search regulatory support Institutional Review Board (IRB) assistance compliance reporting and management of the operations of the research projects. The person will be responsible for providi