Vendor Compliance

Duties: Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams. Manages all technical aspects of GMW document development as well as publishing and archiving activities and is the interface to Global Regulatory Operations. Accountable...

Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams. Manages all technical aspects of GMW document development as well as publishing and archiving activities and is the interface to Global Regulatory Operations. Accountable for...

Job Description: Pay Range $53.05hr - $57.05hr Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams. Manages all technical aspects of GMW document development as well as publishing and archiving...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

Job DescriptionJob DescriptionThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned...

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with...

Job DescriptionJob DescriptionOutside EST ZONE candidate requested not to apply.Duties:Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams. Manages all technical aspects of GMW document development as well as publishing and archiving...

Position Tittle: Medical Technical Writer (Remote) Location: Ridgefield , CT Duration: 12 Plus Months Manages and writes/edits relevant sections of global clinical documents, required for advancing clinical development programs in global, cross-functional study and project teams. Manages all technical aspects of GMW document development as...

Job DescriptionJob DescriptionServpro of Fort Lee s hiring an Accounting & HR Administrator!BenefitsCompetitive compensationSuperior benefitsCareer progressionProfessional developmentAnd more!Key ResponsibilitiesMaintain accurate book keepingCreate financial reports and perform analysisMaintain tax, insurance and compliance requirementsMaintain vendors,...

Job DescriptionJob DescriptionGenesis of Ridgefield is a new entity. Genesis of Ridgefield office staff will work within the BMW of Ridgefield location. BMW of Ridgefield is a premier luxury car dealership dedicated to providing exceptional service and premium automotive experiences to our valued customers. We pride ourselves on our commitment to excellence,...

Congregation Shir Shalom of Westchester and Fairfield Counties, located in Ridgefield, CT is seeking a full-time Director of Finance and Operations to ensure excellent operation of our back office and synagogue. The successful applicant for this full-time on-site position will possess both acute financial skills and experience with day-to-day operational...

Currently, seeking a Clinical Operations Specialist – Technical Support (COS) to join our Business Operations team located at our Ridgefield, CT facility. The COS will provide VBA and SQL programming to existing and new Microsoft Excel workbooks and Microsoft Access databases.This job is a hybrid position with weekly on location visits required in...

Job DescriptionJob DescriptionCurrently, seeking a Clinical Operations Specialist – Technical Support (COS) to join our Business Operations team located at our Ridgefield, CT facility. The COS will provide VBA and SQL programming to existing and new Microsoft Excel workbooks and Microsoft Access databases.  This job is a hybrid position with weekly on...

DescriptionAs an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize...

Clinical Trial Operations (CTO)The CTO will work remotely as a member of the Clinical Trial Team in the Study Management and Conduct Group supporting the Clinical Trial Leader (CTL), Clinical Trial Manager (CTM), and Feasibility Manager (FM). The CTO is responsible for end-to-end site management activities.In addition, may be responsible for supporting the...

Clinical Trial Operations (CTO) The CTO will work remotely as a member of the Clinical Trial Team in the Study Management and Conduct Group supporting the Clinical Trial Leader (CTL), Clinical Trial Manager (CTM), and Feasibility Manager (FM). The CTO is responsible for end-to-end site management activities. In addition, may be responsible for supporting the...