ON SITE RESEARCH STUDY jobs in BOSTON MA, United Kingdom #4

The Clinical Research Coordinator II works within the clinical research program and support the research team in the... regulatory binders and ensures study compliance with all local, state, federal, and IRB requirements. May be responsible for IRB...

Scientific Review Committee and IRB submissions, and site activation activities. 2. Responsible for data reporting..., and archiving of study records, and resolution of data queries. 3. May prepare and or complete regulatory related reports and IRB...

The Clinical Research Coordinator II works within the clinical research program and support the research team in the... regulatory binders and ensures study compliance with all local, state, federal, and IRB requirements. May be responsible for IRB...

study, collates and files forms, documents, and other paperwork to set up and maintain research data (paper and electronic... for research study by reviewing participant data for eligibility; ensures participants referred meet study criteria Establish...

study, collates and files forms, documents, and other paperwork to set up and maintain research data (paper and electronic... for research study by reviewing participant data for eligibility; ensures participants referred meet study criteria Establish...

) assisting Dr. Litz with overseeing the activities of the research assistant and project coordinator assigned to this project... and providing mentorship; (2) scheduling data collection efforts with study collaborators/prison officials and obtaining necessary...

Review Committee and IRB submissions, and site activation activities. Ability to work on multiple research projects... and add responsibilities and tasks as the CRC gains experience. Interest in working on research surrounding cancer treatment side-effects...

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...

Research Assistant II, General Internal Medicine Location: Boston, MA Schedule: 40 hours per week, on-site... aspects of the research study, including: managing program records and handling communication needs of the program. Recruits...

supervising undergraduate research assistants, coordinating testing spaces and study schedules, assisting with preparation...Job Code 403108 Research Assistant I Lab Sub-Unit Social Sciences 052 Time Status Full-time Union 55...

and participates in site visits with the study sponsor to review completeness and accuracy of study documentation Maintains inventory... This position assists in planning and implementing clinical research studies as assigned. Works directly with patients...

study site regulatory binder and essential documents for completeness and accuracy Evaluate ongoing protocol and data...GENERAL SUMMARY/ OVERVIEW STATEMENT: The Program for the Coordination and Oversight of Research Protocols (PCORP...

GENERAL SUMMARY/ OVERVIEW STATEMENT: Working as a part of the Site at the Neurological Clinical Research Institute... subjects participating in the individual research studies such as scheduling patients for research study and collecting...

GENERAL SUMMARY/ OVERVIEW STATEMENT: Working as a part of the Site at the Neurological Clinical Research Institute... subjects participating in the individual research studies such as scheduling patients for research study and collecting...

of education and experience Technical expert in HEOR able to formulate and lead complex research projects ensuring that study... Knowledge of conducting observational research studies; experience with conducting site-based or prospective real-world studies...

study site regulatory binder and essential documents for completeness and accuracy Evaluate ongoing protocol and data...GENERAL SUMMARY/ OVERVIEW STATEMENT: The Program for the Coordination and Oversight of Research Protocols (PCORP...

. Maintain study-related databases, and prepare protocol-related reports as needed. May be responsible for scheduling research..., coordinating and managing site activation, research staff training, regulatory submissions, event tracking and reporting, deviation...