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Debra Lemanski, ABA |
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Mrs. Lemanski has 10 years experience in the pharmaceutical industry. She coordinates GLDD’s regulatory submission and standard operating procedures in accordance with the FDA good clinical practices. In addition, Mrs. Lemanski manages payroll and benefits administration; financial administration; relations with vendors, suppliers, and facilities management; and other operational needs of GLDD. Mrs. Lemanski’s background is primarily in operations and account management including marketing support. She has built her career and experience mainly from manufacturing and marketing companies. Mrs. Lemanski previous experience includes managing the office operations for deCODE Genetics including responsibilities as the Regulatory Affairs Submission Specialist, Off-Site Document Manager and a liaison for virtual due diligence efforts. Mrs. Lemanski received the majority of her administrative training while employed with Pfizer. |
