The Clinical Pharmacy Specialist in GI oncology is responsible for providing clinical pharmacy services to patients in GI Oncology team and will work closely with physicians, mid-l…
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…
About the role Position is on-site in Cambridge, MA #LI-Onsite About the role: We are seeking a highly motivated and innovative Senior Scientist I/II with demonstrated knowle…
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…
Responsibilities Practices as a pharmacist in accordance with all federal, state, DFCI and Joint Commission policies, regulations, and standards. Ensures medication orders and/…
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…
Position: Research Assistant, Hematology/Oncology Location: Boston Medical Center Schedule: 40 hours per week POSITION SUMMARY: The Research Assistant conducts patient recr…
Responsibilities Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of the…