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Home > Department of Radiology Research Administration
Frequently Asked Questions (FAQs)
To submit a question, please contact Eric Tomasini.
About Us
Q: Where are you located?
A: Radiology Research Administration is located at 175 Cambridge Street, Suite 200, Boston MA. Division and Lab administrators sit in their respective areas in Departmental MGH/CNY locations.
Planning | Ordering Research Scans
Q: I received a radiology price quote for a study 2 years ago. I am working on the budget for a new study, can I use the price quotes from 2 years ago?
A: No. Prices change regularly, sometimes by a large margin. Therefore, to ensure adequate budgeting, please contact Radiology Administration before finalizing any budget that includes radiology procedures.
Q: My study requires special imaging protocols. What do I do?
A: Prior to enrolling any patients, you will need to work with Shannon Cahoon, Research Operations Manager, and the Technical Managers to develop a plan of action (i.e. loading IAGs onto machines, naming imaging protocol, special handling, etc.). Without this planning in place, the technologists will not know the special requirements for your study and research subject may be scanned incorrectly.
Administration & Support
Q: I am a Radiologist and was approached by a Pharmaceutical Company to participate in a clinical trial. I need help to get started. Who should I contact?
A: Eric Tomasini, Director, Radiology Research Operations. He will meet with you to review step by step what needs to be completed (i.e. IRB, contracts, MCA, Budget, regulatory, etc)
Q: I have multiple deficits for both Industrial and Sub Contract study funds. I want to correct these accounts. Where do I start?
A: Contact Eileen O'Brien, Manager Finance, and Jeanette Guzman, Financial Analyst. They can help determine the etiology of your deficits, as well show you how to use applications such as Insight and Document Direct to become more proficient in funds management.
Compliance
Q: In terms of clinical trials, what is an FDA Form 1572?
A: This is a Statement of Investigator. No investigator may participate in an investigation until he/she provides the sponsor with a completed, signed Statement of Investigator.
Among other things, by signing this document, you the PI agree to conduct the study(ies) in accordance with the relevant, current protocol(s) and will only make changes in a protocol after notifying the sponsor, except when necessary to protect the safety, rights, or welfare of subjects.
Q: What is Good Clinical Practice?
A: International ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects.
Q: Can I publish as a PI in an Industrial Sponsored, Multicenter Clinical Trial?
A: No, you cannot publish as a PI without permission of the sponsor. Since idea originates with the sponsor, publications lie with sponsor and contributors. However, when awarded a grant, the idea originates with PI, publications lie with MGH PI and contributors.
Education & Research Resources
Q: I am new to Research and would like to learn the basics. What are my options?
A: Review website content, attend monthly RADG meetings, and contact Eric Tomasini, Director, Radiology Research Operations to set up a time to meet. He can tailor an introduction to the department that fits your goals and research interests.
Q: I am not clear on the Post-Award process. Where can I find resources?
A: The Education and Research Resources section of this website has a lot a useful content, including workflows, useful links to research management and tools. You can also contact Eileen O'Brien, Finance Manager for further assistance on managing your funds.
FacultyQ: I am a radiologist in the department and my name is not listed on the radiology research website. Who do I contact?
A: Contact Eric Tomasini, Director, Radiology Research Operations
For any further questions, please contact:
Eric Tomasini
Director, Radiology Research Operations
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