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Cancer and Hematology Clinical Research Program Cancer and Hematology Clinical Research Program

Cancer and Hematology Clinical Research Program - PowerPoint Presentation

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Uploaded On 2022-08-03

Cancer and Hematology Clinical Research Program - PPT Presentation

a nd Translational Research Core About the CHCRP Founded in 1991 Cancer and Hematologybased Trials Cancer Treatment Prevention or Early Detection Symptom Management symptoms caused by disease or by treatments ID: 933997

research cancer clinical bmc cancer research bmc clinical kulke program org compliance patient trials core mahdaviani trc navigation resource

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Slide1

Cancer and Hematology Clinical Research Program

and Translational Research Core

Slide2

About the CHCRP

Founded in 1991Cancer and Hematology-based Trials: Cancer Treatment, Prevention or Early Detection

Symptom Management (symptoms caused by disease or by treatments)Quality of Life of cancer patients

Cancer Care Delivery (examples: Patient Navigation, Disparities, compliance tools)Pre-clinical Research (cellular and molecular studies)

Slide3

Scope of Cancer Research

Cancer Research is not limited to oncology programs. Cancer can be an area of research in many different fields:

All cancer research from ANY department must be reviewed by the cancer program.  This includes any trial involving patients with cancer or trials relating to cancer prevention or detection. Ideally this should be done early in the process

to obtain guidance and to

avoid delays.

IRB applications for all studies involving cancer must be routed to Dr. Kulke in INSPIR for review and sign-off.

Translational Research Core (TRC)

The TRC has recently been developed to allow researchers to obtain specimens and data for their research. Proposals must be submitted to Dr. Kulke for review and approval.

Nutrition

Infectious diseases

PathologyPsychiatryNeurologyGeriatricsPublic HealthOtolaryngologyPharmacySurgeryGenitourinaryGastroenterology

Slide4

How CHCRP can be a resource to others

Infrastructure in place with experience in: Conducting complex clinical trialsRecruiting, consenting and enrolling diverse population utilizing available resources

(interpreter use, patient navigation, individualized participant education, confirming understanding & compliance ability)

Resource utilization – frequent assessment of program needs/workloadsSuccessful audits

Each audit is considered a valuable learning experience, allowing us to incorporate new ideas into our standard procedures Expertise in utilizing Velos

to ensure research billing compliance

Regulatory Requirements

Budget development/anticipating needs

Protocol development (including ICFs, patient materials and protocol coordination tools)

Slide5

Resources

Name

Role

email

Matthew Kulke, MD

Chief, Physician Director

Matthew.Kulke@bmc.org

Salli Fennessey, CCRP

Administrative Director

Sally.Fennessey@bmc.org Anthony Shelton, RNResearch Nurse ManagerAnthony.Shelton@bmc.org Kiana Mahdaviani, PhDTranslational Research Core ManagerKiana.Mahdaviani@bmc.orgNick DangFinancial CoordinatorNhieu.Dang@bmc.org bumc.bu.edu/clinicaltrialsSite is updated monthly and includes:Program Contact InformationCurrent list of active clinical and non-clinical trials

Enrollment and Status Update Forms