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Jacqueline
jakohan@icloud.com
352-327-0792
Gainesville, FL 32653
Registered Nurse
26 years experience W2
0
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Average rating
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Summary

LICENSURE/CERTIFICATION

  • 2015 (current) Registered Nurse RN 9372372 (Compact Multi-State)
  • State of Florida/Department of Health
  • Division of Medical Quality Assurance- Tallahassee, FL
  • 2008 Graduate Certificate in Health Sciences, Clinical Research
  • Administration
  • The George Washington University School of Medicine and Health
  • Sciences - Washington, DC

Experience
Registered Nurse
Medical Devices
Jul 2018 - Apr 2020
  • Registered nurse for Florida state correctional institutes.
  • The RNs are responsible for providing holistic nursing care with appropriate scope of practice to incarcerated patients.
  • Works under the direction of the Director of Nursing and/or Nursing Supervisor and collaborate with a multidisciplinary team to identify, assess and respond to a wide range of physical, psychological and social needs of the patient.
Nursing
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Senior Clinical Research Associate
Medical Devices
Mar 2016 - Jul 2018
Tampa, FL
  • Remote based regional monitor, perform site qualification, site initiation, interim monitoring, and close-out visits.
  • Phase 3 and Phase 1 Acne, Phase 2 PHN.
  • Central point of communication between Sponsor and Investigators for all clinical trial related activities. FSP Sanofi.
No skills were added
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Clinical Research Associate
Medical Devices
Sep 2015 - Mar 2016
  • Contracted as a remoted based monitor to conduct site visits, including site selection, and routine monitoring visits.
  • Phase 1 and 3 Anti-coagulation studies.
  • Direct contract with Sponsor.
No skills were added
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Clinical Research Associate
Medical Devices
Nov 2015 - Mar 2016
Braintree, MA
  • Contracted as a remote based monitor to conduct site visits, from SIV through COV for phase 3 adolescent constipation study.
No skills were added
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Senior Clinical Research Associate
Medical Devices
Mar 2014 - Sep 2015
Tampa, FL
  • Remote based regional monitor, perform site qualification, site initiation, interim monitoring, and close-out visits for Phase 3 and 4 Diabetes and Phase 4 Multiple Sclerosis.
  • Central point of communication between Sponsor and Investigators for all clinical trial related activities.
  • FSP Allergan
No skills were added
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Senior Clinical Research Associate
Medical Devices
Mar 2013 - Jan 2014
North Wales, PA
  • Contracted as remote based monitor; performed routine site visits, including initiation, routine, and close-out visits.
  • Phase 3 Influenza vaccines, adult and pediatric.
  • Protein Science and Novartis.
No skills were added
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Contracted as remote based monitor
Information Technology
Feb 2012 - Mar 2013
  • Contracted as remote based CMA, performed remote clinical monitoring tasks and remote visits for a large Asthma study (Phase 4) in accordance with relevant SOPs, study specific procedures and regulations.
  • Managed/coordinated/supported clinical monitoring activities remotely, including issue resolution, patient enrollment management, handling protocoland/or ICF- and/or contract amendments, drug / supply management and ensuring timely data entry at a site level.
  • Central point of communication between Sponsor and Investigators for all clinical trial related activities.
No skills were added
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Senior Clinical Research Associate (contract)
Information Technology
Sep 2010 - Feb 2012
Durham, NC
  • Contracted as a remote based monitor for studies related to Pulmonary Artery Hypertension (Phase 2), Asthma (Phase 2), and Seasonal Allergic Rhinitis (Phase 3), from study start-up through close-out and routine monitoring.
  • Site manager model, ensured accurate and complete data collection, reviewed paper and electronic medical records.
  • Use of ACT trials and digital pen technology.
No skills were added
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Clinical Research Associate II
Medical Devices
Feb 2008 - Sep 2010
Raleigh, NC
  • Remote based regional monitor for Alzheimer’s study (Phase 3) and chronic low back pain (Phase 3) studies.
  • Reviewed the screening of study participants and performed ongoing monitoring.
  • Ensured accurate and complete data collection.
  • Use of Medidata RAVE and Inform EDC systems.
  • Central point of communication between Sponsor and Investigators for all clinical trial related activities. Janssen, Purdue
No skills were added
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In-House CRA – Study Start-up (contract)
Information Technology
Jul 2007 - Feb 2008
Malvern, PA
  • Contracted as In-House CRA in study start up group for major pharmaceutical developer, conducting review of informed consent, document collection and analysis for regulatory compliance, and site evaluation and approval, non-protocol specific.
Clinical Research Nursing Registered Nurse
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Clinical Research Associate II
Information Technology
Aug 2006 - Jul 2007
East Hanover, NJ
  • Contracted as a remote based monitor for studies related to Multiple Sclerosis (Phase 2-B study), reviewed the screening of study participants and performed ongoing monitoring.
  • Ensured accurate and complete data collection.
  • Use of IMPACT, and home grown EDC system using phone line to upload data, reviewing paper and electronic medical records.
  • Central point of communication between Sponsor and Investigators for all clinical trial related activities.
No skills were added
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Clinical Trial Manager (contract)
Information Technology
Oct 2005 - Aug 2006
East Hanover, NJ
  • Contracted as a CTM for Osteoporosis trial, (Phase 3 study), led end-to-end study efforts across investigator recruiting, site administration and budgets, CRO management, patient enrollment / tracking, data administration, recordkeeping, and study team leadership.
  • Point of contact for study sites and field CRAs, review of CRA visit reports, IVRS reconciliation.
No skills were added
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Safety Nurse - AE narrative composition
Medical Devices
Jun 2004 - Sep 2004
Bala Cynwyd, PA
  • Contracted as a remote based Safety Nurse, composed narratives of adverse events in clinical studies resulting in study discontinuation and serious adverse events, to include in study submissions.
  • Phase 3 birth control and Phase 3 hormone use it men post prostatectomy.
Nursing
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Clinical Study Coordinator- retrospective data collection
Information Technology
Jan 2004 - Jun 2004
Irvine, CA
  • Contracted as a Clinical Study Coordinator for Investigator Initiated lung transplant trial.
  • Performed retrospective data collection, analysis, and validation.
  • Reviewed in-patient medical records for transplant patients in hospital setting, both electronic medical records and paper medical records, transcribed onto paper CRFs.
No skills were added
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Registered Nurse
Medical Devices
Jun 2003 - Aug 2003
Plymouth Meeting, PA
  • Nurse throughout the summer on a weekend only plan in long-term care facility.
Nursing
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Registered Nurse
Information Technology
Jan 2003 - Jun 2003
Somerset, PA
  • Employed on a PRN basis visiting patients in their homes to assess appropriateness of home health care, and provide nursing care.
  • Referred to social services and other disciplines as necessary.
  • Used of OASIS data collection system.
Home Health Nursing
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HEDIS (Health Employer Data and Information Set) Chart Abstractor
Medical Devices
Apr 2003 - May 2003
Hanover, MD
  • Short term contract for collection of data for HEDIS for Pedigree Healthcare Services.
  • Traveled to physician’s offices and reviewed selected charts on selected diagnoses, entered data in HEDIS, a quality rating system used by the insurance industry.
HEDIS
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Community Health Nurse
Medical Devices
Apr 2002 - Jan 2003
Somerset, PA
  • Public Health Nurse at state health center serving Cambia County.
  • Provided immunizations, tracked and reported infectious disease, provided education and treatment for TB, provided HIV counseling and testing, collected and shipped birds for testing for West Nile Virus.
  • Handled case management of PKU and high lead level clients.
  • Used NEDSS database for disease reporting.
Home Health Nursing Case Management
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Medical Program Coordinator
Chemicals/Pharmaceuticals
Feb 1998 - Feb 2000
Johnstown, PA
  • On site Medical Program Coordinator for a CNS therapy to treat / prevent Alzheimer’s disease (Phase 3 studies), performing extensive review of clinical trial data, and coordination of subject retention efforts, site communications, SAE resolution, and adverse event adjudication process coordination.
  • Provided direct assistance to clinical study investigators and contributed to regulatory compliance review of study documents.
  • Played key role in EDC system testing and launch, home grown Oracle based system.
  • Encoded medical terms for both trials using sponsor dictionaries
Case Management Nursing
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Medical Program Coordinator
Medical Devices
Aug 1996 - Mar 1998
Blue Bell, PA
  • On site clinical data reviewer. Reviewed clinical trial data from paper CRFs and computer line listings.
  • Generated data queries and worked with sites to resolve data questions.
  • Worked with clinical and statistical teams to clean data and prepare tables for submission.
No skills were added
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Drug Safety and Information Specialist
Information Technology
Mar 1997 - Aug 1997
Horsham, PA
  • Fielded professional and layman questions and concerns regarding a new Multiple Sclerosis drug in marketing phase.
  • Drug was marketed after trial demonstrated it slowed the progression of MS.
  • Through telephone interview process, assessed and recorded data regarding adverse events, coded according to FDA dictionaries.
  • Provided emotional support to MS patients and their significant others, provided information regarding the disease process.
No skills were added
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Registered Nurse
Information Technology
Oct 1996 - Apr 1997
  • Registered nurse for a non-profit psychiatric hospital that specialized in crisis stabilization and referral.
  • Ensured patient safety, suggested and encouraged appropriate behavior, monitored and reported effects of therapy, provided therapeutic environment, and administered routine and PRN medications.
Nursing Psychiatric
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Registered Nurse
Healthcare
Jan 1995 - Jun 1996
Norristown, PA
  • Staff nurse on cardiopulmonary medical floor, provided hands on nursing care and supervised nurse’s aides.
  • Also worked on a PRN basis for the hospital’s home health agency, providing nursing care to patients in their homes.
Nursing Psychiatric Home Health
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Edit Skills
Non-cloudteam Skill
Education
Health Sciences, Clinical Research Administration
The George Washington University 2011
Nursing
Florida Atlantic University 1996
Nursing
Indian River Community College 1994
Villanova University 1984
Arts
Florida Keys Community College 1981
Skills
Nursing
2020
7
Case Management
2003
2
Home Health
2003
2
Psychiatric
1997
1
Clinical Research
2008
1
HEDIS
2003
1
Registered Nurse
2008
1