Mary Art Email & Phone Number | Highly effective Senior Clinical Trials Project Manager with consistent achievement in study initiation, management, and closeout. Manage the requirements of the customer, needs of the business, and technical constraints involved in the oversight of multiple clinical studies. Certified Clinical Research Associate (CRA); strong knowledge of FDA and ICH Guidelines, Good Clinical Practices (GCP’s), and Quality System Regulations (QSR’s) / Good Manufacturing Practices (GMP’s) Experience with multiple site management systems including Electronic Data Capture and Clinical Trial Management Systems Strong communication, organization, and planning skills; able to work independently while managing competing projects and deadlines Therapeutic areas: Diabetes (I & II), Diabetic Macular Edema, Psoriasis, Osteoporosis, Hypercholesterolemia, Benign Prostatic Hyperplasia (BPH), and Erectile Dysfunction Previous experience in Regulatory Affairs, Quality Assurance, and Product Development including technical writing, GMP audits, and project management

Mary Art

Highly effective Senior Clinical Trials Project Manager with consistent achievement in study initiat...
Monument, Colorado, United States

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Mary Art’s Location Monument, Colorado, United States

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Mary Art’s Prior Industry Quintiles | Eli Lilly

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Senior Project Manager – Endocrine and Neuroscience

2016-04-01T00:00:00.000Z - Present

Clinical Trials Project Manager / Clinical Lead

2009-06-01T00:00:00.000Z - 2016-03-01T00:00:00.000Z

Senior Clinical Research Associate – Endocrine, Women’s Health, and Neuroscience

2001-08-01T00:00:00.000Z - 2008-10-01T00:00:00.000Z

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Mary Art is a Highly effective Senior Clinical Trials Project Manager with consistent achievement in study initiation, management, and closeout. Manage the requirements of the customer, needs of the business, and technical constraints involved in the oversight of multiple clinical studies. Certified Clinical Research Associate (CRA); strong knowledge of FDA and ICH Guidelines, Good Clinical Practices (GCP’s), and Quality System Regulations (QSR’s) / Good Manufacturing Practices (GMP’s) Experience with multiple site management systems including Electronic Data Capture and Clinical Trial Management Systems Strong communication, organization, and planning skills; able to work independently while managing competing projects and deadlines Therapeutic areas: Diabetes (I & II), Diabetic Macular Edema, Psoriasis, Osteoporosis, Hypercholesterolemia, Benign Prostatic Hyperplasia (BPH), and Erectile Dysfunction Previous experience in Regulatory Affairs, Quality Assurance, and Product Development including technical writing, GMP audits, and project management