A Real Estate Development and Property Management company is seeking a Regional Project Manager for various locations throughout our investment portfolios.This individual will be primarily responsible...
read moreA Real Estate Development and Property Management company is seeking a Regional Project Manager for various locations throughout our investment portfolios.This individual will be primarily responsible...
read moreLegal Operations Manager (Data Analyst).In this role, you will be responsible for rate analysis, rate approvals, and invoice review and approval.You’ll also track key legal metrics, develop reports an...
read moreLegal Operations Manager (Data Analyst).In this role, you will be responsible for rate analysis, rate approvals, and invoice review and approval.You’ll also track key legal metrics, develop reports an...
read moreEffectively assess Keyword Research and Content Optimization projects and be able to provide quality checks to ensure keywords are appropriate for a given project’s URL list.
Effectively assess Keyword Research and Content Optimization projects and be able to provide quality checks to ensure keywords are appropriate for a given project’s URL list.
Cultural Lead & Operations - Marketing/Advertising.
Cultural Lead & Operations - Marketing/Advertising.
We are seeking a Project Coordinator to support the successful delivery of a high-end luxury residential project in Staten Island for a well-established White Plains-based general contractor.This role...
read moreWe are seeking a Project Coordinator to support the successful delivery of a high-end luxury residential project in Staten Island for a well-established White Plains-based general contractor.This role...
read moreUS 22, Springfield Township, NJ 07081.Generous Pay Plan + Great Benefits!.Pay is negotiable with experience!.Receptionist experience is preferred but not required.Enjoy working in our BEAUTIFUL dealer...
read moreWe are seeking a dedicated Project Coordinator with a sharp focus on construction-related tasks.The candidate should be capable of managing multiple projects, demonstrating exceptional communication s...
read moreUS 22, Springfield Township, NJ 07081.Generous Pay Plan + Great Benefits!.Pay is negotiable with experience!.Receptionist experience is preferred but not required.Enjoy working in our BEAUTIFUL dealer...
read moreWe are seeking a dedicated Project Coordinator with a sharp focus on construction-related tasks.The candidate should be capable of managing multiple projects, demonstrating exceptional communication s...
read moreInnova Solutions is immediately hiring for a IT Project Manager V >.Position type: Contract/Fulltime.Mode: Hybrid (3 days onsite in a week).In-depth knowledge of and experience in the financial indust...
read moreInnova Solutions is immediately hiring for a IT Project Manager V >.Position type: Contract/Fulltime.Mode: Hybrid (3 days onsite in a week).In-depth knowledge of and experience in the financial indust...
read moreHybrid Role- Candidates must be local and commutable to client sites in Raritan, NJ or Horsham, PA.Full Time position offering Joulé Benefits and PT.
Hybrid Role- Candidates must be local and commutable to client sites in Raritan, NJ or Horsham, PA.Full Time position offering Joulé Benefits and PT.
Minimum of 5 years of clinical research administration related experience including extensive experience in trial study start-up, coverage analysis, clinical trial budgeting, financial disclosures, IR...
read moreMinimum of 5 years of clinical research administration related experience including extensive experience in trial study start-up, coverage analysis, clinical trial budgeting, financial disclosures, IR...
read moreReporting to the Senior Scientist at and working in collaboration with the SFARI Data & Biospecimens Repository (SDBR) and Informatics Teams, the Clinical Research Specialist will support various data...
read moreReporting to the Senior Scientist at and working in collaboration with the SFARI Data & Biospecimens Repository (SDBR) and Informatics Teams, the Clinical Research Specialist will support various data...
read moreThe ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. Reporting to the Regulatory Aff...
read moreThe ACC One Cancer Clinical Research (OCCR) is instrumental in the development and implementation of cancer clinical trials that offer cutting-edge oncology treatments. The ACC OCCR Regulatory Affairs...
read moreThe Clinical Research Quality Specialist must verify the site is conducting the trial in compliance with the approved protocol. The CR Quality Specialist C is responsible for performing GCP compliance...
read moreThe CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the ...
read moreThe CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the ...
read moreThe CR Quality Specialist C is responsible for performing GCP compliance activities for sponsored IND clinical research trials and Investigator initiated trials to verify human subjects are safe, the ...
read moreThe NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory queries, and participate in the initiation of the new study, as well as, communi...
read moreThe NCI/NCTN Senior Regulatory Affairs Start-Up Specialist is expected to resolve, with minimal supervision, regulatory queries, and participate in the initiation of the new study, as well as, communi...
read moreOversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific cou...
read moreOversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific cou...
read moreThe Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinic...
read moreThe Clinical Research Data Specialist supports the data collection, analysis and reporting functions for the Office of Clinical Research (OCR) for assigned oncology trials in Phase I, II or III clinic...
read moreMinimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ ex...
read moreMinimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ ex...
read moreMinimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ ex...
read moreMinimum of seven years of experience as a clinical research monitor/auditor, research nurse or research coordinator with at least three years’ experience directly monitoring/auditing or five years’ ex...
read moreThe Clinical Research Specialist serves as a regulatory expert and resource for investigators and others within the Clinical Research Support Office in the Hospital. The Clinical Research Specialist c...
read moreThe Clinical Research Specialist serves as a regulatory expert and resource for investigators and others within the Clinical Research Support Office in the Hospital. The Clinical Research Specialist c...
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