Office of Data Quality (ODQ) Contact List
Mailboxes | |
iRIS and OncPro Activation
| Email: ODQActivation@dfci.harvard.edu |
CRF Data / InForm EDC
| Email: ODQDataManagement@dfci.harvard.edu |
OnCore Subject Registration
| Email: ODQ@dfci.harvard.edu For urgent issues, please call the ODQ registration line at 617-632-3761. |
Policies and Education
| Email: ODQEducation@dfci.harvard.edu |
iRIS Navigation
| Email: DFHCCiRISNavigator@dfci.harvard.edu |
Clinical Trial Registration & Reporting
| Clinicaltrials.gov Email: DFCIODQClinicalTrialsGov@partners.org CTRP Email: ODQCTRP@partners.org
|
DSMC and DSMB
| Email: ODQDataSafety@dfci.harvard.edu |
LEADERSHIP | |||
 | Amy Clark Associate Director, Clinical Research Systems | Oversees ODQ Feasibility & Activation in IRIS | |
 | Nareg Grigorian | Oversees Auditing & DSMB/DSMC | |
 | Claire Sulkowski Manager, Clinical Trials Education | Manages DF/HCC Policies & Training Requirements | |
 | Kathya Yadama Manager, Data Quality | Oversees Data Management of InForm Trials | |
Auditing & Data and safety monitoring | |||
 | Teresa Alati Clinical Research Auditor | ||
 | Neli Azimi Clinical Research Auditor | ||
 | Prince Bosque-Hamilton Clinical Research Auditor | ||
 | Sharon Kobelin Clinical Research Auditor | ||
 | Grace Lachance | ||
 | Belinda Lee-Clarke Program Coordinator | Coordinates Audit Committee & DSMB/DSMC | |
ctrp/clinicaltrials.gov | |||
 | Rachel Bent Clinical Trial Registration Coordinator | Clinicaltrials.gov Registration & CCSG Reporting | |
 | Janet Coletti Clinical Trial Registration Coordinator | Clinicaltrials.gov Registration & CCSG Reporting | |
 | Tess Aucoin | ||
Data Management | |||
 | Dan Beardslee Data Quality Analyst | ||
 | Annette Dalton Data Quality Analyst | DFCI Acute Lymphoblastic Leukemia Consortium (ALL) & Sickle Cell | |
 | Caroline Green Data Quality Analyst | ||
 | Jocelyn McCarthy Data Quality Analyst | ||
 |
May Okiwe
| ||
 | Beth Byrd | ||
Education/Training & NCI REgistration Support | |||
 | Olivia Wood Clinical Trials Education Coordinator | CITI HSP/GCP and General DF/HCC Training Support | |
Registration and Activation | |||
 | Paul Burke Lead Clinical Research Systems Specialist | Subject Registration & Randomization | |
 | Jesus Chacin Chirino | iRIS Feasibility & Subject Registration | |
 | Kate Gildea Clinical Research Systems Specialist | iRIS Navigation | |
 | Laura Gillis Clinical Research Systems Specialist | Activation & OncPro | |
 | Jon McCurdy Clinical Research Systems Specialist | iRIS Feasibility | |
 | Leslie Rawles Clinical Research Systems Specialist | Activation & OncPro | |
 | Danielle Shaffer Lead Clinical Research Systems Specialist | Activation & OncPro | |
 | Chavonne Dunbar | ||