Resumes
Resumes

Regulatory And Clinical Consultant, Medical Devices
View pageLocation:
2470 Barbaro Dr, Memphis, TN 38134
Industry:
Medical Devices
Work:
Farage Consulting since Apr 2010
Regulatory / Clinical Consultant, Medical Devices
InSet Technologies May 2009 - Mar 2010
Sr. CRA
St. Jude's Children's Research Hospital Jan 2009 - May 2009
Clinical Research Monitor II
Quintiles, Inc May 2007 - Jan 2009
Sr. Clinical Research Associate
MetaCure, USA Sep 2005 - May 2007
Clinical Research Associate
Regulatory / Clinical Consultant, Medical Devices
InSet Technologies May 2009 - Mar 2010
Sr. CRA
St. Jude's Children's Research Hospital Jan 2009 - May 2009
Clinical Research Monitor II
Quintiles, Inc May 2007 - Jan 2009
Sr. Clinical Research Associate
MetaCure, USA Sep 2005 - May 2007
Clinical Research Associate
Education:
University of Mississippi 1981 - 1984
Masters; of Art, Health Care Administration; Psychology University of Mississippi 1977 - 1984
MHCA, Health Care Administration
Masters; of Art, Health Care Administration; Psychology University of Mississippi 1977 - 1984
MHCA, Health Care Administration
Skills:
Clinical Research
Clinical Trials
Medical Devices
Regulatory Affairs
Fda
Regulatory Submissions
Clinical
Clinical Monitoring
Pma
Clinical Trial Management
Orthopedics
Diabetes
510 K
Pain Management
Gcp
Edc
Protocol Development
Irb
Ide
Compliance
Ctms
Orthopedic
Validation
Regulatory Requirements
Cardiology
Quality Assurance
Clinical Development
Clinical Data Management
Therapeutic Areas
Vaccines
Cro
Protocol
Sop
Data Management
Medical Writing
Neurology
Biotechnology
Pharmaceutical Industry
Drug Development
21 Cfr Part 11
Ich Gcp
Good Clinical Practice
U.s. Food and Drug Administration
Clinical Trials
Medical Devices
Regulatory Affairs
Fda
Regulatory Submissions
Clinical
Clinical Monitoring
Pma
Clinical Trial Management
Orthopedics
Diabetes
510 K
Pain Management
Gcp
Edc
Protocol Development
Irb
Ide
Compliance
Ctms
Orthopedic
Validation
Regulatory Requirements
Cardiology
Quality Assurance
Clinical Development
Clinical Data Management
Therapeutic Areas
Vaccines
Cro
Protocol
Sop
Data Management
Medical Writing
Neurology
Biotechnology
Pharmaceutical Industry
Drug Development
21 Cfr Part 11
Ich Gcp
Good Clinical Practice
U.s. Food and Drug Administration
Interests:
Product Liability
Good Monitoring Practices
Reforming Medical Device Research
Clinical Trial Workshop
Statistics For Non Statisticians
Good Monitoring Practices
Reforming Medical Device Research
Clinical Trial Workshop
Statistics For Non Statisticians
Languages:
English
Certifications:
Rac