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Conducting Clinical Trials

  • Updated: 06/03/2013

Appendices 8 - 10

Appendix 8: Cover Letter from Dr. Jeff Abrams
Appendix 9: Planning Committee and Government Advisors to the Committee 
Appendix 10: Working Group Rosters

Appendix 8: Cover Letter from Dr. Jeff Abrams, February 15, 2012

Appendix 9: Planning Committee and Government Advisors to the Committee NCI Concise Informed Consent Template Project - February 2013

CCR/NIH
Christine Grady, RN, PhD, Deputy and Acting Chief, Department of Bioethics, Clinical Center
Caryn Steakley, RN, MSW, Deputy Clinical Director, Center for Cancer Research (CCR)

CDP/ DCTD/NCI
Tracy Lively, PhD, Associate Chief, Diagnostics Evaluation Branch, Cancer Diagnosis Program (CDP)

CIP/ DCTD/NCI
Barbara Galen, MSN, CRNP, CNMT, Program Director, Cancer Imaging Program (CIP)
Frank Lin, MD, Medical Officer, Clinical Trials Branch, CIP

CTEP/ DCTD/NCI
Jeff Abrams, MD, Associate Director, Cancer Therapy Evaluation Program (CTEP)
Jeanne Adler, RN, MPH, CCRP, Nurse Consultant, Clinical Investigations Branch, CTEP
Meg Mooney, MD, Branch Chief, Clinical Investigations Branch, CTEP

DCCPS/NCI
Sandra Mitchell, PhD, CRNP, Research Scientist and Program Director, Outcomes Research Branch, Applied Research Program, Division of Cancer Control and Population Sciences (DCCPS)
Wendy Nelson, PhD, MPH, Program Director, Basic and Behavioral Research Branch, Behavioral Research Program, DCCPS

DCP/NCI
Leslie Ford, MD, Associate Director, Clinical Research & Acting Deputy Director, Division of Cancer Prevention (DCP)
Kathleen Foster, RN, BA, Nurse Specialist, Clinical Trials, DCP
Marge Good, RN, BSN, MPH, OCN, Nurse Consultant, Community Oncology and Prevention Trials Research Group, DCP
Lori Minasian, MD, FACP, Acting Director, DCP
Diane St. Germain, RN, MS, CRPNP, Nurse Consultant, Community Oncology and Prevention Trials Research Group, DCP
Judy Smith, RN, MSN, AOCN, Nurse Consultant, Lung and Upper Aerodigestive Cancer Research Group, DCP

Office of the NCI Director
Shannon Bell, MSW, Former Director, Office of Advocacy Relations
Steven Krosnick, MD, Program Director, Coordinating Center for Clinical Trials (CCCT)
Jean Lynn, RN, MPH, OCN, Program Director, CCCT
Kelli Marciel, MA, Director, Office of Advocacy Relations
Rose Mary Padberg, RN, MA, Public Health Advisor for Clinical Trials, Office of Communications and Education (OCE)
Geriann Piazza, MA, Technical Writer/Editor, OCE

NCI Support Contractor (EMMES)
Rebecca Enos, RN, MPH

Government Advisors to the Planning Committee

FDA
Sandra Casak, MD, Staff Fellow, Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA)
Ruthann Giusti, MD, Medical Officer, CDER, FDA
Shan Pradhan, MD, Medical Officer, CDER, FDA

OHRP
Jerry Menikoff, JD, MPP, MD, Director, Office for Human Research Protections (OHRP)
Julie Kaneshiro, Team Leader, Policy, OHRP
Lisa Rooney, Compliance Oversight, OHRP
Lisa Buchanan, Compliance Oversight, OHRP

Appendix 10: Working Group Rosters: NCI Concise Informed Consent Template Project - February 2013