Product Liaison Manager

• Jan 2023 - Present

Florence advances clinical research through software. Florence eBinders replace paper investigator site files, trial master files and source binders with a shared platform to speed clinical trial work between trial sites and sponsors.

Sr. Account Relationship Manager

• Jul 2021 - Jan 2023

Account Relationship Manager

• Aug 2020 - Jul 2021

Manager, Project Operations

• May 2019 - Aug 2020

Peachtree BioResearch Solutions is a full-service Clinical Research Solutions Organization that specializes in providing clinical development services to biotechnology, pharmaceutical, and medical device companies – focusing on emerging to mid-sized companies. PBRS teams are comprised of subject matter experts who are able to contribute at high levels beyond their core functional area. Peachtree BioResearch Solutions is a full-service Clinical Research Solutions Organization that specializes in providing clinical development services to biotechnology, pharmaceutical, and medical device companies – focusing on emerging to mid-sized companies. PBRS teams are comprised of subject matter experts who are able to contribute at high levels beyond their core functional area.

Clinical Project Manager

• Jan 2018 - May 2019

GlobalCare Clinical Trials delivers high quality and convenient clinical trial services in the home or alternate-site setting in support of phase I-IV clinical trials in a variety of therapeutic areas, genomics and personalized medicine in all age groups. GlobalCare Clinical Trials delivers high quality and convenient clinical trial services in the home or alternate-site setting in support of phase I-IV clinical trials in a variety of therapeutic areas, genomics and personalized medicine in all age groups.

Clinical Trial Management System (CTMS) Budget Migration Specialist

• Sep 2017 - Dec 2017

* Cross-referenced cancer center budgets with contract, payment terms, coverage analysis, protocol, and informed consent to ensure consistency while escalating errors found through synchronization process for budget renegotiation * Created financial and operational framework of clinical studies in the CTMS and extracted and synthesized billable items from oncology clinical trial agreements for input into OnCore Clinical Trial Management system * Proactively identified areas of improvement within CTMS and provided vendor with enhancement requests to improve functionality Show less

Lead Clinical Research Coordinator

• Apr 2015 - Jul 2017

* Led an interdisciplinary team of four research coordinators, one research medical assistant, and two data coordinators* Evaluated protocol deviations and serious adverse events and develops corrective action plans * Performed quarterly in-house monitoring of the quality of data provided in electronic case report forms (eCRFs) while verifying source documents for accuracy* Formulated standard source documentation to be used in conjunction with electronic medical records so that instructions for site staff are deliberate, clear, and sustainable* Acted as liaison between research site and third party vendors, including contract research organizations and data management interfaces* Served as a subject matter expert on over thirty clinical trials and disseminates information and best practices by conducting weekly presentations to the research team and other key stake holders * Managed the clinical aspects of research protocols phases (I-IV) from site selection through completion* Cross-referenced protocol budgets with study calendars to ensure source documentation and IBM Clinical Trial Management System accuracy in order to ensure costs related to subject visits were billed appropriately Show less

Clinical Research Coordinator

• May 2013 - Apr 2015

* Explained all aspects of the clinical trial to the patient, distilling complex medical terms to relatable language, and documented the informed consent process* Proactively coordinated and scheduled study related tests and procedures to ensure protocol compliance and deadlines were met* Maintained all study records within the electronic medical record in accordance with Good Clinical Practice* Identified, aggregated, and presented protocol, patient, and general study issues to primary investigator in weekly clinical meetings* Evaluated and interpreted research protocols to ensure compliance from both patients and treating physicians* Oversaw training and performance of the laboratory team to ensure tests were performed as ordered* Experience with Epic and Varian Electronic Medical Records Show less

Clinical Research Coordinator

• Mar 2012 - May 2013

* Supervised and trained junior and senior staff on participant recruitment and scheduling, biomedical sample processing, proper documentation, identifying and documenting adverse events, and variances * Reviewed medical histories of potential subjects; consented, interviewed and screened participants to determine eligibility prior to study enrollment * Organized and updated preliminary subject data using Excel and SPSS in preparation for later analysis * Ensured financial records remained up to date in order to manage billing services and patient compensation * Maintained regulatory binder which included preparation of regulatory documents and compilation of current CVs, medical licenses, study contact information, CITI training certifications, and delegation of authority log * Led the preparation for a study audit and responsible for timely response to auditor’s requests and questions * Created and performed ongoing review of standard operating procedures for all study-related procedures Show less

BMT and Lymphoma Clinical Trial Working Group Intern

• Jan 2011 - Dec 2011

* Organized research materials and oversaw research data management * Learned the fundamental strategies behind the management of clinical research and the healthcare industry * Organized research materials and oversaw research data management * Learned the fundamental strategies behind the management of clinical research and the healthcare industry