Do you need assistance in managing your pharmaceutical research trials?
Are
you searching for an experienced trial monitor?
Could your projects benefit by having someone who is experienced
in teaching GCP and regulatory issues?
My name is
Dana Hoskins and I am an independent registered nurse consultant working in the field of
pharmaceutical research and device testing. I am available to assist you and your associates with your clinical research projects
should you require an experienced trial manager and monitor.
My medical background includes a wide experience in
the fields of medical/surgical, critical care, home health nursing, and clinical research performed in a university setting.
I was a research trial coordinator for the University of Louisville School of Medicine for several years.
In 1985,
I started a Contract Research Organization and Consulting business Florida Clinical Research. I have operated FCR for over
twenty years.
In 1986, I started and directed all aspects of an Institutional Review Board. I offered its services
nationally from 1986 through 1999.
Throughout the past twenty years I have worked on over fifty-one trials for
more than thirty different pharmaceutical companies. I have worked from coast to coast in the United States as well as working
in five different countries throughout the world.
I would like to offer my experience and services to you and
your associates for your new upcoming projects. I am also available to assist with any ongoing projects that may require additional
independent support and project management.
I have extensive experience in teaching
and lecturing toprofessional associations, medical schools and universities nationally and internationally
in the following areas:
In-house
services offered to Pharmaceutical Companies include assistance with:
Good Clinical Practice (GCP)Issues
FDA Regulations and Requirements
IRB and
Regulatory Issues
Budget Planning and Proposals
Identification of Research Investigators
Initiation of
New Research Sites
Training/Updates for Research Investigators
Planning/Initiation of New Research Offices
Training/Updates
for Study Coordinators
Training for Study Support Personnel
Database Reconciliations
Regulatory Document Tracking
Site/Sponsor Correspondence Reconciliation
Adverse
Event Coding/Database Reconciliation
Assist with writing of protocols and informed
consents