Marisa Pagano Rn Email & Phone Number | RN licensed in New Jersey and Tennessee. Extensive, diverse experience in Clinical and Pre-Clinical pharmaceutical studies. Experienced in all stages of Phase I, II, and III clinical trial studies ranging from site feasibility, quarterly budget forecasting, study maintenance and archiving activities. Maintaining organized, audit ready, site study files to be provided to CRAs for monitoring visits. Experienced in generating Rave Medidata patient visits reports and making payments to sites. Maintain detailed Investigational Product Tracking Tables for studies, including initiating manual drug shipments, as well as using IVRS. Proficient in quality checking federal and site documents and preparing studies for archiving. Expansive knowledge in electronic Trial Master File uploading and reconciliation for Clinical Trial Portal and Vault. Participated in numerous internal and external study audits and addressed findings. Extensive experience with the CTMS Impact and Spectrum. Specific expertise in data collection systems, including Rave Medidata, Access, Catalyst, Business Objects, Shared Investigator Platform (SIP).

Marisa Pagano Rn

RN licensed in New Jersey and Tennessee. Extensive, diverse experience in Clinical and Pre-Clinical...
Nolensville, Tennessee, United States

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Marisa Pagano Rn’s Email marisa.pagano@spcorp.com

Marisa Pagano Rn’s Phone Numbers

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Marisa Pagano Rn’s Location Nolensville, Tennessee, United States

Marisa Pagano Rn’s Current Industry Icon Strategic Solutions

Marisa Pagano Rn’s Prior Industry Pra Health Sciences | Merck | Huntingdon Life Sciences

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In-House CRA 2

2021-06-01 00:00:00 - Present

In-House CRA 2

2015-10-01 00:00:00 - 2021-06-01 00:00:00

Associate Biologist

2006-10-01 00:00:00 - 2015-10-01 00:00:00

Large Animal Technician

2005-06-01 00:00:00 - 2006-09-01 00:00:00

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Marisa Pagano Rn is a RN licensed in New Jersey and Tennessee. Extensive, diverse experience in Clinical and Pre-Clinical pharmaceutical studies. Experienced in all stages of Phase I, II, and III clinical trial studies ranging from site feasibility, quarterly budget forecasting, study maintenance and archiving activities. Maintaining organized, audit ready, site study files to be provided to CRAs for monitoring visits. Experienced in generating Rave Medidata patient visits reports and making payments to sites. Maintain detailed Investigational Product Tracking Tables for studies, including initiating manual drug shipments, as well as using IVRS. Proficient in quality checking federal and site documents and preparing studies for archiving. Expansive knowledge in electronic Trial Master File uploading and reconciliation for Clinical Trial Portal and Vault. Participated in numerous internal and external study audits and addressed findings. Extensive experience with the CTMS Impact and Spectrum. Specific expertise in data collection systems, including Rave Medidata, Access, Catalyst, Business Objects, Shared Investigator Platform (SIP).