Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Provide administrative support to Research Nurses in clinic setting. Responsible for basic clinical trial document preparation (informed consents, study drug diaries, surveys (electronic/paper), research specimen kits, etc.) Administer clinical trial related surveys and use validated tools to assess a trial participant's functional and cognitive abilities as required by t

Facilitate human research studies through sample and data collection and coordination. Utilize REDCap, OncCore, Excel and other hospital information systems and statistical software analysis tools to perform clinical research and outcomes data analysis for research publications. Manage various databases from multiple labs generating clinical and biological data of tumor a

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Serve as a study contact for a few longitudinal clinical research studies Prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study regulatory binders, enter all required study data on an ongoing basis. Screen, recruit, and enroll eligible patients and track participation over time (including some travel to Dana Farber's Londonder

Primary responsibility will include management and maintenance of clinical and research databases and assistance with chart and database abstraction. Recruitment and consent of patients for enrollment on research studies Oversight of the research study start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activati

Oversight of research study start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data q

The successful candidate will have proven experience in managing and independently executing complex bioinformatics tasks in the frame of Bioinformatics Workbench project. The role's responsibilities will include Owning and leading various projects, serving as a subject matter expert. Developing and implementing bioinformatics tools and pipelines in cloud environment. Col

Reporting to the Director of Biosafety, the Associate Biosafety Officer maintains the integrity of the DFCI Biosafety and Import/Export Controls Compliance Programs and support for the DFCI research program and pharmacy USP797 sterile compounding program. This includes being the administrator for the Institutional Biosafety Committee (IBC), the overall Biosafety and Biose

Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group's clinical trial portfolio and all related regulatory and compliance requirements. The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group's p

Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group's clinical trial portfolio and all related regulatory and compliance requirements. The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group's p

The Research Assistant for the EdAssistConsulting Solutions Team is an Internship making sure that the information in team data repositories is current, organized, and accurate. They gather the data from client workforce education policies,databases, spreadsheets, and other documents and organize it in spreadsheets and document files. The Research Assistant will also need