Office of Data Quality (ODQ) Contact List

 

Mailboxes

 

iRIS and OncPro Activation

  • OncPro document posting

  • Eligibility Checklists
  • iRIS conditions from ODQ Feasibility and ODQ Activation
  Email: ODQActivation@dfci.harvard.edu 

CRF Data / InForm EDC

  • General data management questions
  • Missing forms reports
  • Data requests
 Email: ODQDataManagement@dfci.harvard.edu 

OnCore Subject Registration

  • Centralized protocol registration
  • Randomized, PI-initiated trial registration

Email: ODQ@dfci.harvard.edu

For urgent issues, please call the ODQ registration line at 617-632-3761.

Policies and Education 

  • HSP/GCP Training (CITI)
  • New Investigator Training
  • New Multi-Center Sponsor Training
  • DF/HCC Policies/Operations
 Email: ODQEducation@dfci.harvard.edu

iRIS Navigation

  • Bundling or submission of multiple amendments in parallel

 Email: DFHCCiRISNavigator@dfci.harvard.edu

Clinical Trial Registration & Reporting

  • ClinicalTrials.gov records
  • CTRP records

Clinicaltrials.gov Email: DFCIODQClinicalTrialsGov@partners.org

CTRP Email: ODQCTRP@partners.org

 

DSMC and DSMB 

  • Data Safety Monitoring Committee/Board
 Email: ODQDataSafety@dfci.harvard.edu

LEADERSHIP
 

 Amy Clark
Manager, Clinical Research Systems 		 (617) 632-3769
Email		 iRIS Feasibility & Activation
 

 Nicholas Farley
Director		 (617) 632-3731
Email

 
 

Nareg Grigorian
Manager, Data and Safety Monitoring

 (617) 582-8656
Email		 Auditing & DSMB/DSMC 
    

ADMINISTRATION
 

 Lenette Ranger
Administrative Specialist		 (617) 632-4347
Email		  
 

 Belinda Lee-Clarke
Administrative Specialist		 (617) 632-3763
Email		 Audit Committee & DSMB/DSMC
    

Auditing

      
 

 Teresa Alati
Clinical Research Auditor		 (617) 582-7547
Email		  
 

 Neli Azimi
Clinical Research Auditor		 (617) 632-5813
Email		  
 

 Prince Bosque-Hamilton
Clinical Research Auditor		 (617) 632-8320
Email		  
 

 Sharon Kobelin
Clinical Research Auditor		 (617) 632-2601
Email		  
 

 Trang Vo
Clinical Research Auditor		 (617) 632-4751
Email		  
    

ctrp/clinicaltrials.gov
 

 Rachel Bent
Clinical Trial Registration Coordinator		 (617) 582-8318
Email 		 Clinicaltrials.gov Registration & CCSG Reporting
 

 Janet Coletti
Clinical Trial Registration Coordinator		 (617) 632-2114
Email 		 Clinicaltrials.gov Registration & CCSG Reporting
    

Education
 

 Claire Sulkowski
Education Coordinator		 (617) 582-8422
Email		 Training Requirements & DF/HCC Policies
    

Data Management
 

 Annette Dalton
Data Quality Analyst		 (617) 632-3842
Email         		 DFCI Acute Lymphoblastic Leukemia Consortium (ALL) & Sickle Cell
 

 Caroline Green
Data Quality Analyst		 (617) 632-8319
Email		  
 

 Dan Beardslee
Data Quality Analyst		 (617) 632-3026
Email		  
 

 Kathya Yadama
Data Quality Analyst		 (617) 632-3762
Email		  
    

Registration and Activation
 

 Paul Burke
Lead Clinical Research Systems Specialist 		 (617) 632-6719
Email		 Subject Registration & Randomization
 

 Max Danielsson
Clinical Research Systems Specialist 		 (617) 632-2551
Email		 iRIS Feasibility 

Kate Gildea
Clinical Research Systems Specialist 		 (617) 582-7423 
Email		 iRIS Navigation
 

 Laura Gillis
Clinical Research Systems Specialist 		 (617) 632-6279
Email		 Activation & OncPro
 

 Jon McCurdy
Clinical Research Systems Specialist 		 (617) 582-7266
Email		 iRIS Feasibility
 

 Peter O'Neil
Clinical Research Systems Specialist 		 (617) 582-8661
Email 		  Activation & OncPro
 

 Leslie Rawles
Clinical Research Systems Specialist 		 (617) 632-2238
Email		  Activation & OncPro
 

 Danielle Shaffer
Lead Clinical Research Systems Specialist 		 (617) 632-5133
Email 		  Activation & OncPro