Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Administrative: Assists principal investigator with protocol development. Assists principal investigator as appropriate with the Institute’s protocol review p…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
GENERAL SUMMARY/ OVERVIEW STATEMENT: A Clinical Research Coordinator I position is available within the Department of Radiation Oncology. The Clinical Research Assistant works …
GENERAL SUMMARY/ OVERVIEW STATEMENT: A Clinical Research Coordinator I position is available within the Department of Radiation Oncology. The Clinical Research Assistant works …
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Coordinate data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archivi…
The Clinical Research Coordinator II works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice…
The Clinical Research Coordinator II works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice…
When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Coordinate data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archivi…
Responsibilities Oversight of the clinical trials start-up process for site activation activities. Responsible for data reporting and management, collection of source documents…
Responsibilities Screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort studies. Interact with study participants as direc…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
Responsibilities Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation act…
The Clinical Research Coordinator I (CRC) works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Pra…
The Clinical Research Coordinator I (CRC) works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Pra…
The Clinical Research Coordinator I (CRC) works within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Pra…