Experience

Wake Research
• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee
• Lead Clinical Research Coordinator

  • Apr 2021 - Present


Collaborative Neuroscience Network LLC.

• 1 - 100 Employee

• Clinical Study Coordinator

  • Jun 2015 - Apr 2021

  Responsible for: Helping with clinical research organizational aspects such as patient management, data collection, electronic/written data entry, preparing source documents for doctor review, preparing source documents, lab kits, medication kits for patient visits, maintaining lab supplies/study supplies for each individual study, monitoring the lab in the processing of study specific samples, contacting the patients to remind them of their visits and checking on their progress.▪ Also responsible for: Consenting patients and caregivers, constructing master source and site-specific study binders for multiple studies, preparing for monitoring visits, answering data queries, constructing enrollment logs, monitoring enrollment and providing enrollment updates to outreach, investigators, sponsors and senior study coordinators, scheduling, and maintaining working relationships with patients.▪ Assists with: Vitals, processing urine/blood laboratory tests, acting as doctor’s point person. practicing phlebotomy and taking ECGs during clinic hoursTherapeutic Experience:Schizophrenia, Schizoaffective Disorder, Bipolar Disorder, Major Depressive Disorder, Healthy Volunteers Show less

• Data Management Coordinator

  • Sep 2013 - Jun 2015

  ▪ Responsible for: Managing a small team to ensure proper data collection, entry and query resolution for all 45+ studies on site, preparing weekly reports on all data entry activity to report to Site Manager, training staff on how to use different EDC systems, working with CRAs and site CRCs to maintain EDC access for the research team, completing electronic/written data entry and query resolution on multiple studies, constructing master source and site-specific study binders for multiple studies, preparing for routine IMVs, constructing enrollment logs, completing monthly enrollment log review for all studies and ensuring all subject visits are entered correctly into Clinical Conductor.▪ Also responsible for: Assisting with clinical research organizational aspects such as patient management, preparing source documents for doctor review, preparing source documents, lab kits, medication kits for patient visits, maintaining lab supplies/study supplies for each individual study, monitoring the lab in the processing of study specific samples, contacting the patients to remind them of/ schedule their visits and check on their progress. ▪ Assists with: Vitals, processing urine/blood laboratory tests, acting as doctor’s point person. practicing phlebotomy and taking ECGs during clinic hours. Show less

• Research Assistant/Data Management

  • May 2007 - Sep 2013

  ▪ Responsible for: Helping with clinical research organizational aspects such as patient management, data collection, electronic/written data entry, preparing source documents for doctor review, preparing source documents, lab kits, medication kits for patient visits, maintaining lab supplies/study supplies for each individual study, monitoring the lab in the processing of study specific samples, contacting the patients to remind them of their visits and checking on their progress. ▪ Also responsible for: Constructing master source and site-specific study binders for multiple studies, preparing for monitoring visits, answering data queries, constructing enrollment logs, scheduling and maintaining working relationships with patients.▪ Assists with: Vitals, processing urine/blood laboratory tests, acting as doctor’s point person. practicing phlebotomy and taking ECGs during clinic hours. Show less

• Clinical Research Coordinator

  • Dec 2009 - Jul 2010

  ▪ Responsible for: Helping with clinical research organizational aspects such as patient management, data collection, electronic/written data entry, preparing source documents for doctor review, preparing source documents, lab kits, medication kits for patient visits, maintaining lab supplies/study supplies for each individual study, monitoring the lab in the processing of study specific samples, contacting the patients to remind them of their visits and checking on their progress.▪ Also responsible for: Consenting patients and caregivers, constructing master source and site-specific study binders for multiple studies, preparing for monitoring visits, answering data queries, constructing enrollment logs, monitoring enrollment and providing enrollment updates to outreach, investigators, sponsors and senior study coordinators, scheduling, and maintaining working relationships with patients.▪ Assists with: Vitals, processing urine/blood laboratory tests, acting as doctor’s point person. practicing phlebotomy and taking ECGs during clinic hours.Therapeutic Experience:Schizophrenia, Schizoaffective Disorder, Bipolar Disorder, Major Depressive Disorder, Alzheimer’s Disease, Parkinson’s Disease Show less



Calscience Environmental Laboratories, Inc.

• Chemist

  • Jun 2005 - May 2007

  ▪ Responsible for: Analyzing water and soil samples using GC/MS while following QC procedures and EPA methods, organizing and checking data reports, GC/MS machine maintenance, making liquid internal standards. ▪ Responsible for: Analyzing water and soil samples using GC/MS while following QC procedures and EPA methods, organizing and checking data reports, GC/MS machine maintenance, making liquid internal standards.



Sav-ons

• France
• Chemical Manufacturing

• Pharmacy Clerk

  • Sep 2004 - Nov 2004

  ▪ Responsible for: Cashiering, stocking medication, dispensing medication ▪ Responsible for: Cashiering, stocking medication, dispensing medication