CURRICULUM VITAE PRESENT POSITION:
Board-Certified Dermatologist Lubbock Dermatology and Skin Cancer Center
ADDRESS: POSTGRADUATE
TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER, Lubbock, Texas
TRAINING:
Dermatology Residency - July 1997 – June 2000
UNIVERSITY OF TEXAS MEDICAL BRANCH, Galveston, Texas
Pediatric Internship - June 1996 - June 1997
GRADUATE EDUCATION:
UNIVERSITY OF TEXAS MEDICAL BRANCH, Galveston, Texas
Doctor of Medicine with Honors, August 1992 - May 1996
UNDERGRADUATE
ANGELO STATE UNIVERSITY, San Angelo, Texas
EDUCATION:
Bachelor of Science, August 1987 - May 1991 - magna cum laudePROFESSIONAL
Texas State Board of Medical Examiners - 1998
LICENSURE:
BOARD CERTIFICATION:
American Board of Dermatology, October 2000
PROFESSIONAL
American Academy of Dermatology, Fellow, 2000 - present
ORGANIZATIONS:
Texas Dermatological Society, Member 2001 - present
American Medical Association, 1994 - present
Texas Medical Association, 1992 - present
Lubbock-Crosby-Garza Medical Society, 1997 -present
American Society for Lasers in Surgery and Medicine, 2002-present
Alpha Omega Alpha, University of Texas Medical Branch, 1995
Gold-Headed Cane Award nominee, University of Texas Medical Branch, 1996
Alpha Chi Honor Scholarship Society, Angelo State University, 1990
Who's Who Among Students in American Universities and Colleges, Angelo
COMMUNITY SERVICE:
American Academy of Dermatology annual skin-cancer screenings, 1998 – present
Lubbock Community Health Center annual skin-cancer screening, 2001-present
Lubbock City Health Department skin-cancer screening, 1999
Lubbock Cooper High School skin-cancer screening, 1999
RESEARCH:
Rapini RP, Clark JW: A double-blind, randomized, placebo controlled,
multicenter, parallel group evaluation of the efficacy and safety of sertaconazole 2% cream on patients with interdigital tinea pedis.
Butler DF, Clark, JW: A 26-week study with a 6-week randomized multicenter, double-blind, vehicle-controlled,
parallel-group phase followed by a 20-week, open-label phase to study the safety and efficacy of 1% SDZ ASM 981 cream in pediatric subjects with atopic dermatitis.
Phase IV Open-label, observational cohort study – Assessment and Tracking of long-term
Phase IV 12 week open-label, observation study to evaluate adapalene gel 0.1% as part of a
Combination therapy regimen in moderate to moderately severe acne 2006
Phase IV Open-label 4 week trial to evaluate patient satisfaction with clobetasol proprionate
0.05% when used as monotherapy or as add-on therapy for the treatment of
Phase III Multi-Center, randomized, double-blind, parallel-group study to demonstrate the efficacy and safety of adapalene/benzoyl peroxide topical gel compared with adapalene topical gel, 0.1%; benzoyl topical gel, 2.5% and topical gel vehicle in subjects with acne vulgaris.
Phase IV Observational Post-Marketing Safety Surveillance Registry of etanercept for the treatment
Phase III randomized, double-blind, multiple-site, placebo controlled, parallel design, clinical study
to evaluate the bioequivalence of generic Adapalene Gel 0.1% compared to brand adapalene 0.1%
1. Clark JW, 9/6/98, Santa Fe, New Mexico, "Generalized Lichen Planus", Southwestern Dermatological Society
2. Clark JW, Butler DF, Rapini RP, 5/8/99, Dallas, Texas, "Uncommon Presentations of Langerhans Cell
Histiocytosis", Texas Dermatological Society Spring Meeting
3. Clark JW, Butler DF, Bang R, 3/10/00, San Francisco, California, "Fatal Sporotrichosis", Gross and Microscopic
Symposium, 58th Annual Meeting of the American Academy of Dermatology
4. Clark, JW, 3/6/02, Lubbock, Texas, “Warts and Acne”, Pediatric Grand Rounds, Covenant Medical Center 5. Clark, JW, 5/31/02, Lubbock, Texas, “Atopic Dermatitis”, Pediatric Symposium, Covenant Medical Center
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