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 
 

Kathya Yadama
Manager, Data Quality
(617) 632-3762
Email
Data Management of InForm Trials
    

ADMINISTRATION

 

Lenette Ranger
Administrative Specialist
(617) 632-4347
Email
 NCI Investigator Registration (RCR)
 

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
 
    

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