Clinical Research Support

Clinical Trials Education Office (CTEO)

Research Education Series

This continuing education series for study staff focuses on ethical issues in clinical resarch, barriers to day-to-day trial management and clarifications about how to apply regulations and guidelines to current practice. The series schedule is posted on a quarterly basis.

Registration is strongly encouraged and can be done by accessing the on-line registration form located at the end of each session description.

Contact the CTEO at CTEO@dfci.harvard.edu if you have any questions or would like more information.

DF/HCC Clinical Research Policy Update
Upcoming Session Date: **DATE CHANGE** August 15, 2008 10am-11am DANA 1620
Register

DF/HCC and Cancer Care in 2015
Personalized cancer medicine is our Cancer Center's Evantual care goal. Realizing this vision will require a number of important institutional changes that will affect the way we do basic and clinical research. This session will provide a glimpse of things to come.
Presented by Barrett Rollins, MD, PhD, Chief Scientific Officer for Dana-Farber Cancer Institute
August 22, 2008 10am-11am Dana 1620 Register
This session will also be videobroadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room

Effective Trial Managment Series: PI-Initiated, In-House Trials
Upcoming Session Date: September 12, 2008 10am-11am Dana 1620 Register
This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room

PI-Initiated Multi-Center Trials: Guidance for Researchers and Staff
Upcoming Session Date: September 26, 2008 10am-11am Dana 1620 Register
This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room

Source Documentation Practices
Source documentation is the basis for all trial data. It respects and protects study participants, and backs up the investigator and study team. Through a series of case studies, this session will review source documentation requirements and the means by which the requirements can be met.
Upcoming Course Date: October 10, 2008 10am-11am Dana 1620 Register
This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room

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Clinical Research Support Clinical Trials Education Office (CTEO) Research Education Series Research Education Series This continuing education series for study staff focuses on ethical issues in clinical resarch, barriers to day-to-day trial management and clarifications about how to apply regulations and guidelines to current practice. The series schedule is posted on a quarterly basis. Registration is strongly encouraged and can be done by accessing the on-line registration form located at the end of each session description. Contact the CTEO at CTEO@dfci.harvard.edu if you have any questions or would like more information. DF/HCC Clinical Research Policy Update Upcoming Session Date: DATE CHANGE *August 15, 2008 10am-11am DANA 1620* Register DF/HCC and Cancer Care in 2015 Personalized cancer medicine is our Cancer Center's Evantual care goal. Realizing this vision will require a number of important institutional changes that will affect the way we do basic and clinical research. This session will provide a glimpse of things to come. Presented by Barrett Rollins, MD, PhD, Chief Scientific Officer for Dana-Farber Cancer Institute August 22, 2008 10am-11am Dana 1620 Register This session will also be videobroadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room Effective Trial Managment Series: PI-Initiated, In-House Trials Upcoming Session Date: September 12, 2008 10am-11am Dana 1620 Register This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room PI-Initiated Multi-Center Trials: Guidance for Researchers and Staff Upcoming Session Date: September 26, 2008 10am-11am Dana 1620 Register This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room Source Documentation Practices Source documentation is the basis for all trial data. It respects and protects study participants, and backs up the investigator and study team. Through a series of case studies, this session will review source documentation requirements and the means by which the requirements can be met. Upcoming Course Date: October 10, 2008 10am-11am Dana 1620 Register This session will also be video broadcast to MGH CCPO 326 Cambridge St. 2nd Floor Conference Room	Office for Human Research Studies (OHRS) Quality Assurance Office for Clinical Trials (QACT) Clinical Research Unit (CRU) Clinical Trials Education Office (CTEO) Templates for Investigator-Initated Research Workshops Clinical Investigator Education Series Human Subject Protection Training (CITI) Research Education Series Education on Demand National Protocol Registration NCI Investigator Registration Guide to Human Research Activities Tips & Tricks Contacts Protocol Review and Monitoring System (PRMS)
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