- Merck & Co. (Rahway, NJ)
- … Trial -Assistant, Study Coordinator , Regulatory CTC ( Clinical Trial Coordinator ) or similar.MRLGCTO#EligibleforERPETJOBSNOTICE FOR INTERNAL ... relationships and ensures continuity of site relationships through all-phases of the trial .Performs clinical study site management/ monitoring activities in… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders.Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in the West, in ... adherence to Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...are created in a timely manner (communication plan, site monitoring plan, etc) ahead of study start. Oversee CRO… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in...the study and propose mitigation plans.Monitor study budget against trial progress and bring deviations to the Operational program… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics and share with study team, ... and immune disorders.SummaryThe incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... around rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more
- Vitalief (Newark, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient… more
- New York University (New York, NY)
- …provide full-time intervention support on Systems Aligning for Equity (SAFE) Spaces, a clinical randomized control trial funded by The National Institute of ... Coordinator include: + Supporting management and organization of clinical and study data + Supporting student coach/trainee recruitment, on-boarding,… more
- Weill Cornell Medical College (New York, NY)
- …Under direction, monitors all data management, regulatory and financial aspects of clinical trial operations. This role also coordinates special research ... Title: Research Coordinator Location: Upper East Side Org Unit: Comp...projects, prepares internal board protocols for clinical research, assists in the design of evaluation tools/instruments… more
- RWJBarnabas Health (Somerville, NJ)
- …RWJUH Somerset, 110 Rehill Ave, Somerville, NJ 08876 Job Overview: Research Coordinator for a Dynamic and Expanding Outpatient Oncology Research Department. The ... to multitask on a variety of projects Preferred: + Clinical Research experience Scheduling Requirements: + Day Shift +...+ Acts as a liaison with study sponsors, scheduling monitoring visits and conference calls, and providing timely responses… more
- Weill Cornell Medical College (New York, NY)
- …Under direction, monitors all data management, regulatory and financial aspects of clinical trial operations. This role also coordinates special research ... projects, prepares internal board protocols for clinical research, assists in the design of evaluation tools/instruments and coordinates budgets. **Job… more
- Merck (Rahway, NJ)
- …across the different local country roles ensuring a strong collaboration (including the CTC Clinical Trial Coordinator , CRAs and COM Clinical Operations ... Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). + Responsible for project management of the… more
- Merck (Rahway, NJ)
- …Clinical Trial Assistant, Study Coordinator , Regulatory CTC ( Clinical Trial Coordinator ) or similar. **MRLGCTO** **\#EligibleforERP** **ETJOBS** ... through all phases of the trial . + Performs clinical study site management/ monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws &… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... rare diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more
- Weill Cornell Medical College (New York, NY)
- …**Experience** Approximately 5 or more years of related research experience in clinical trial management. **Knowledge, Skills and Abilities** + Knowledge of ... Title: Clinical Research Project Manager Location: Upper East Side...Completes all WCM regulatory submissions including Protocol Review and Monitoring Committee (PRMC), Institutional Review Board (IRB), Data Safety… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... rare diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more
- HSS (New York, NY)
- …research budgets with sponsors for new studies and amendments. + Primary contact for clinical trial budget creation; oversees finances related to the clinical ... 2+ years of clinical research experience and comprehensive understanding of the clinical trial process + Proficiency in Microsoft Office suite + Excellent… more
- Hackensack Meridian Health (Hackensack, NJ)
- …audits, as well as ensuring ongoing compliance of study-related documentation throughout the clinical trial lifecycle for all assigned clinical trials. ... the Medicare Coverage Analysis, budget and contract for a clinical trial in order to initiate a...+ Certified Clinical Research Professional or Certified Clinical Research Coordinator or Society of … more
