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Date Created: 12/22/15
__________________________Roxanne Thomas_________________________ firstname.lastname@example.org 323-754-9144 Professional Excellence Self-motivated, business oriented, and customer-focus driven Strong effective interpersonal skills – ability to motivate and empower others to achieve a desired action; ability to communicate on various divisions/levels Proficiency in public speaking – effective verbal, oral, and written communication Strong computer and internet skills including knowledge of MS-Office products (Excel, Word, PowerPoint) Professional Experience 1993- 2012 Neutrogena Corporation Los Angeles, CA 90047 Responsibilities Respected professional working in the role as a specialist on fundamental operations that pertain to Clinical Research under title of Principal Research Technician: Clinical Operations logistics: Execute internal studies to support clinical operations: activities include initiate communications with external study sites, protocol GCP review, source document review, informed consent preparation/review, eligibility criteria, study protocol, questionnaire development and study guidelines. Work with specific groups (regulatory affairs, clinical supplies, formulations, and business counterparts) to coordinate product releases during the safety transition period. Conduct Safety testing Recruit qualified subjects for skin sensitivity (sting) testing Manage and streamline process for payments of clinical safety studies which include timely generation of purchase orders, issuance of debit memos, and accurate targeting of charge-back. Incorporate critical GCP elements in clinical trials: ICH Compliance – Adherence to SOP-005427, substitution of top-line excel calculations with internal study report Report and document Adverse Events Assist claims leaders to develop innovated claims: Make sure timelines are met for artwork by monitoring study activities - include product shipment status, subject recruitment, enrollment and scheduling process, preliminary data availability and monitoring/communication complications. Provide timely feedback to formulators, claims, and management- via email, telephone, and franchise database updates Increase Scientific Affairs operational efficiency: Work with IT/ Clinical Supplies to optimize GMC and release timelines Work with Clinical Supplies Release Technicians to support internal compliance initiatives, and 2011 FDA Monograph requirements Work closely with Toxicology to provide information necessary for preservative decisions Work closely with Formulations to optimize testing conditions Work closely with safety and formulations team to ensure timely fielding and delivery of feedback Posters/Presentations 1997 American Academy of Dermatology “High Glycerin Therapeutic Moisturizers – A Retrospective Analysis of Treating Dry Skin During Winter Clinicals: 1991-1996” 2007 21 World Congress of Dermatology “High Glycerin Hand Cream Provides Relief from Occupational Dermatitis In Coal Miners” Work History 1988-1980 World of Curls, Inc. – Carson, CA Simon & Schuster/Gulf Western Corporation – Bristol, PA Carter-Wallace, Inc. – Cranbury, NJ Johnson & Johnson Baby Products – Skillman, NJ Education 2007- 2009 University of Phoenix BS – Business Management Military 1985-1990 United States Air Forces – Honorable Discharge McGuire AFB, NJ
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