Vanessia J. Twillie

*** ********* **

Memphis, TN 38109

acpjsx@r.postjobfree.com

Phone: 901-***-****

MANAGEMENT AND ORGANIZATION DEVELOPMENT

Excellent communication skills, motivational, critical thinking, problem-solving skills, notable training skills,

Detail-oriented, multitasking, organized, extensive knowledge in clinical trials, developing and troubleshooting

analytical methods

CORE COMPETENCIES

Good Laboratory Practices (GLP) Good Clinical Practices (GCP) Good Manufacturing Practices (GMP)

Laboratory Safety Committee High Performance liquid Chromatography (HPLC) Empower Liquid

Chromatography with a tandem of mass spectrometry (LCMS) Method Development Writing of Report and

Standard Operation Procedures (SOP's) Microsoft Words and Excel

WORK EXPERIENCE

1 Record Management & Decommissioning Specialist, Kelley Scientific-

2 (MGM Integrated Solution) 12/2014 –present

Knowledge of Good Records Management Practices & Policies

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Maintain record logs and indexes to provide status of information and retrieval

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Perform accurate identification, classification and inventory of records, equipment, systems and

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applications in any format or medium

Identify records eligible for destruction

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Inventory and audit GMP and Non-GMP records

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Drug Enforcement Agency (DEA training)

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3 Research Associate -Senior Research Associate I, (GTx Inc.) 02/2007 -10/2013

Led analysis of Bio-analytical (biological samples including plasma, serum and blood) study samples

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using liquid chromatography with tandem mass spectrometry (LCMS) in support of drug discovery,

nonclinical and clinical study samples.

Led method development and validation of the LCMS methods for GTx proprietary new chemical

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entities, using protein precipitation and LLE methodologies.

Responsible for daily use and maintenance of the LCMS instruments, troubleshot instrument

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problems.

Wrote and reviewed standard operating procedures, and both non-glp and glp reports.

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Led implementation of ordering system of analytical laboratories… laboratories maintained daily

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operation.

Member of the GTx Safety Committee…strengthened skills to ensure safety and efficacy of products

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Qcing of data interpretation that ensured the data was creditable for FDA reporting.

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Led analysis of the drug discovery sample analysis, including sample receipt, method development,

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and analysis and reporting of results.

Oversaw laboratory supplies and ordering, ensured laboratory maintained daily operations

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Reviewed and updated the standard operating procedures…

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Vitamin Analyst, (Eurofin Laboratory) 01/2002-02/2007

Responsible for setting up runs of over a 10,000 different types of samples (including: food product

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and animal feed) on the High Performance Liquid Chromatography (HPLC) using the Agilent.

Sorted and prioritized samples to keep reporting due date

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Reported data for various Vitamins test (Vitamins A, E, C, B1 and B2 ) in support of nutrition labels.

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Ran samples using Gas Chromatography (GC) using Chem-Station software.

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Cell culture experience in running Vitamin B assays

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Calculated weights for samples to accurately quantified the concentration of vitamins in sample

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composition

Responsible for setting up samples on the HPLC run on the system using empower software

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EMPLOYMENT HISTORY

2002 - 2007 Vitamin Analyst– Eurofins Scientific Laboratory-Memphis, TN

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2007 - 2009 Research Associate I – Gtx Inc.- Memphis, TN

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2009- 2013 Senior Research Associate I – Gtx Inc.-Memphis, TN

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2014-Present Record Management & Decommissioning Specialist- Merck-Memphis, TN

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EDUCATION

High School Diploma: George Washington Carver High School- Memphis, TN (1996)

Bachelor of Science in Biology- Lane College -Jackson, TN (2000)

SPECIALIZED TRAINING

AB Sciex LCMS training

Empower Software

Chem-station

Cardiopulmonary Resuscitation (CPR) training

Respiratory face mask fitness testing training

Tomtec

Good Laboratory Practice (GLP)

Good Clinical Practice (GCP)

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