Consolata Uzzi

** ***** ****** *********, *** Jersey 07040

Phone: 201-***-****. E-mail: acvten@r.postjobfree.com

EDUCATION (with Honors and Awards):

American University of Antigua School of Medicine Sept. 2008 – Feb. 2013

Doctor of Medicine

Rutgers University, Newark, NJ. Sept. 2004 - May 2006

BSc (Biology)

Honors College, Rutgers University

Who is who among American College Students

PROFESSIONAL EXPERIENCE:

Alfa Consulting Solutions

Travel CDI specialist /Medical reviewer Apr. 2013- Apr. 2016

Assist physicians with improving medical record documentation.

Assist physicians in determining pathophysiology of disease.

Understanding of pharmacology and therapeutics.

Knowledge of International and US Regulatory Requirements

Ensure intensity of services is accurately reflected in medical record.

Instructs staff on proper documentation in the medical record.

Ensure resolution of queries prior to patient’s discharge.

Actively participate and assist Performance Improvement Department in

documentation for compliance in quality of care measures for specific charts.

Provide appropriate orientation and ongoing education for coding staff

Serve as a central resource for inpatient and ambulatory coding questions

Perform inpatient/hospital coding

Celgene Pharmaceuticals Summit NJ Jan. 2008 - Aug. 2008

Drug safety specialist

Retrieved case initial and date stamp source document

Copied and sent source documents to Clinical Operations for clinical Serious adverse event

Checked initial source document for completeness.

Generated concise, accurate and well-written case narratives

Responsible for the efficient development of the safety management plan.

Effectively maintained the safety database and corresponding entry guidelines, including accurate entry of data and assurance of quality of data through quality control process.

Performed consistent coding of diseases, adverse events, and medications.

Supported the generation of Annual Safety Updates, Periodic Safety Reports, and other cumulative safety reports including data retrieval, analyses and quality control.

Reconciled SAEs in accordance with project specific guidelines

Schering-Plough Research institute Springfield, NJ Jun. 2007 Dec. 2007

Quality Control Analyst/ Reviewer

Performed quality control checks for GPV-CARES (Global Pharmacovigilance Safety Database) Data entry fields that impact expedited ICSRs and aggregate reports for correctness and completeness.

Performed medical review on domestic and international clinical trial and adverse event reports on marketed products.

Maintenance of the company’s adverse event database.

Responded to inquiries and requests for safety information from health professionals worldwide

Reviewed and analyzed safety data for risk assessment, labeling changes or other safety-related actions.

Pfizer Global Pharmaceutical Morris Plains, NJ May 2006 May 2007

Pharmacovigilance Analyst

Created adverse events safety database from source documents and spontaneous and clinical trial adverse event reports

Prepared clinical narrative when indicated while maintaining consistency with the global adverse event database

Responsible for determining seriousness of cases in collaboration Drug safety specialist officers

Oversaw the archiving, filling, and organization of sponsored Clinical Trial Files, Help Desk Support, and retrieving requested information

Assisted in archiving Patients Files and Trial Master Files (TMF)

Public Health Research Institute Newark, NJ Jan 2006 –Apr. 2006

Research Assistant

Worked with experienced PhD’s on the study of Trypanosoma Brucei the causative agent of sleeping sickness in humans and Nagna disease in cattle

Experimented with different techniques to isolate tbTBP protein from the organism and to check for its solubility in E-coli

Performed different molecular biology techniques, such as preparing western blots, Polymerase Chain Reaction (PCR), making agarose gel and others

CURRENT LICENSURE/ CERTIFICATION:

ECFMG certified, BLS and ACLS certified C-CDS.

COMPUTER and DATA SKILLS:

Clinical Database; (Trial Master File), Argus, ARIGs, Microsoft Office Suite, SABA, Oracle Documentum, Medra Coding, Inpatient/hospital coding.

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