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If you are a participant in Medical or Social Research or are thinking about being a participant, I can help you regarding your rights and what to expect as a "research subject". It is important to know what to expect. For one thing, your consent form as the gateway to your particpation. You need to know if this is valid.

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Volunteer

Rosemarie Price

Expertise

My over 20 years experience enables me to answer questions relating to Research Consent in Medical Research. Subject's rights are not discussed enough and it is an area the general public is not aware of in that great effort and many FDA and institutional guidelines and rules carry the ethics in which research is guiding the individuals experience in research.

Experience

Varied experience (Institutional Review Board Administrator and Board Participant, Research Monitor, Research Coordinator, Clinical Trial Data Manager, Research Interviewer) in many forms of research; cancer clinical trials; Alzheimers Disease; psychiatric adolescent research and epidemiology (colon and lung cancer). I have created protocols and carried them out in the field, the hospital setting and on the phone and in the field as an interviewer. I have been an administrator in three NYC Institutional Review Boards, reviewing protocols with knoweledge of the FDA research regulations. Also, I have been on the Institutional Review Board of a well known university hospital here in NYC. Most recently, created a Standard of Practice for a Department of Orthopaedics here in NYC as a Department Research Coordinator.

Organizations
ACRP; Association of Clinical Research Professionals

Education/Credentials
BA in Sociology from CUNY. Various certificates including Good Clinical Practices, Alzheimers Cognitive Impairment Scale among others

Past/Present Clients
Columbia Univesity, Mount Sinai Hospital, St. Luke's-Roosevelt Hospital

Encyclopedia

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