| SANDRA M. NERO Education: |
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| Erie Community College, North, 1972-1974 Williamsville, New York Associate Degree in Applied Science (Medical Office Assistant) |
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| Experience: |
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| SUZANNE BRUCE AND ASSOCIATES, P.A. The Center for Skin Research 1900 St. James Place, Suite 650 Houston, Texas 77056 Clinical Research Coordinator |
March 2000 - Present |
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| BAYLOR COLLEGE OF MEDICINE Department of Dermatology Houston, Texas Senior Clinical Study Coordinator Clinical Study Coordinator) Responsibilities: Coordinated all activities associated with the preparation and conduct of Dermatology clinical research studies. Served as key liaison between pharmaceutical sponsors and/or their representatives and study site investigators, including support personnel. Reviewed proposed protocols, prepared study budgets, prepared protocol applications and patient informed consent forms for submission to IRB, prepared advertisements and public service announcements for patient recruitment, coordinated support facilities/personnel, screened potential study patients on telephone and in clinic, took medical histories and vital signs, assisted investigator during patient visits, dispensed study medication and patient instructions, scheduled patient appointments, completed case report forms and generated source documents, reconciled data queries, organized and maintained all study regulatory files. Trained and supervised coordinator assistants. May 1999: Successfully completed an FDA Routine Field Inspection for Data Validation for Hyal Pharmaceuticals' actinic keratoses study (primary site, top enroller). While at Baylor, have coordinated clinical studies for the following dermatological indications: acne, actinic keratoses, atopic dermatitis, eczema, herpes genitalis/labialis/zoster, hirsutism, photo-damage (including solar lentigines and wrinkles), psoriasis, skin structure infections, tinea corporis/ cruris/pedis, urticaria, venous stasis leg ulcers. |
1991- March 2000 1988 - 1991 |
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| BRISTOL-MYERS SQUIBB PHARMACEUTICAL RESEARCH INSTITUTE WESTWOOD PHARMACEUTICALS INC. Buffalo, New York Administrative Clinical Research Assistant Bristol-Myers Pharmaceutical R&D Division Department of Clinical Research Responsibilities: Coordinated administrative activities and served as key liaison with study site personnel (assured proper implementation of research protocols, initiated and reviewed documentation necessary for the timely initiation and orderly progress of clinical studies, assisted with monitoring ongoing studies, conducted batchfield edits). Study coordinator of in-house clinical research studies (prepared ads for patient recruitment, screened patients, coordinated facilities, scheduled patient appointments, dispensed medications and patient instructions, prepared all documents). Administratively, coordinated grant information, maintained adverse drug experience report files, maintained physician/consumer files. Department Secretary Bristol-Myers Pharmaceutical R&D Division Department of Clinical Research Executive Secretary Bristol-Myers Pharmaceutical R&D Division Westwood Pharmaceuticals Inc. R&D Administration Secretary/Senior Secretary Westwood Pharmaceuticals Inc. Department of Pharmacology/Toxicology |
1987 - 1988 1983-1987 1982-1983 1977-1982 |
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| STATE UNIVERSITY OF NEW YORK AT BUFFALO Department of Psychiatry Buffalo, New York Stenographer Division of Community Psychiatry |
1974-1977 |
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| Community Service: |
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| Provide photoeducation to student and adult populations during community health fairs. |
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| Professional Membership: |
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| Dermatology Nurses Association | ||
713.985.0210