... support responsible financial management of clinical trials with Clinical Research Coordinators.Collaborate with Data Coordinator(s) to assure the documentation for the clinical trial is complete and accurate; assist ...
... in northern New Jersey.The Clinical Research Coordinator I serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive ...
... integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a ... data management activities within a clinical trial, as well as leading and ...
... Jersey.Reporting to the Lombardi Clinical Trials Office (Lombardi CTO) Training, Education, and Quality Control Manager, the Quality Control Coordinator I will interface with various ...
... contract amendment(s) preparation. Sending trial materials documents to the sites. Entering data in the Clinical Trial Management System (CTMS). Ensures appropriate ... , Excel, and PowerPoint. Experience in clinical trials is preferred. Ability to learn ...
... of in-house and remote Clinical Research Associates (CRAs) and Clinical Trial Coordinators (CTCs). * Ensure compliance with pertinent ...
... of in-house and remote Clinical Research Associates (CRAs) and Clinical Trial Coordinators (CTCs). * Ensure compliance with pertinent ...
... the necessary medical contribution to clinical trial protocols and prepare relevant documentation ... -functional teams involved in the clinical trial programs within Boehringer Ingelheim. You ...
... .General Description:The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines ... timely completion of oncology hematology clinical trials within the assigned region.Identify ...
... possess: At least 5 years clinical monitoring experience and or relevant clinical trial experience. Relevant life science degree ...