Resumes
Resumes
Associate Director, Clinical Operations, Evlp Development
View pageLocation:
Washington, DC
Industry:
Pharmaceuticals
Work:
Lung Biotechnology Pbc United Therapeutics Corporation
Associate Director, Clinical Operations, Evlp Development
Medimmune Jan 2007 - Jun 2007
Associate Director, Investigator-Initiated Trials, Medical and Scientific Affairs
Medimmune Nov 2005 - Jan 2007
Associate Director, Medical Affairs Operations
Medimmune Jan 2005 - Nov 2005
Senior Clinical Program Manager, Clinical Operations
Associate Director, Clinical Operations, Evlp Development
Medimmune Jan 2007 - Jun 2007
Associate Director, Investigator-Initiated Trials, Medical and Scientific Affairs
Medimmune Nov 2005 - Jan 2007
Associate Director, Medical Affairs Operations
Medimmune Jan 2005 - Nov 2005
Senior Clinical Program Manager, Clinical Operations
Education:
Fairleigh Dickinson University 1992 - 1995
Master of Business Administration, Masters University of Pittsburgh 1984 - 1988
Bachelors, Bachelor of Science, Psychology, Chemistry
Master of Business Administration, Masters University of Pittsburgh 1984 - 1988
Bachelors, Bachelor of Science, Psychology, Chemistry
Skills:
Clinical Trial Management
Infectious Diseases
Vaccines
Biotechnology
Clinical
Medical Education
Therapeutic Areas
Clinical Trials
Clinical Research
Clinical Development
Gcp
Pharmaceuticals
Sop
Edc
Clinical Monitoring
Pharmaceutical Industry
Oncology
Ctms
Medical Affairs
Pharmaceutics
Drug Development
Regulatory Affairs
Pharmacovigilance
Cro
Clinical Data Management
Regulatory Submissions
Clinical Operations
Fda
Medical Writing
U.s. Food and Drug Administration
Electronic Data Capture
Standard Operating Procedure
Good Clinical Practice
Clinical Trial Management System
Cro Management
Infectious Diseases
Vaccines
Biotechnology
Clinical
Medical Education
Therapeutic Areas
Clinical Trials
Clinical Research
Clinical Development
Gcp
Pharmaceuticals
Sop
Edc
Clinical Monitoring
Pharmaceutical Industry
Oncology
Ctms
Medical Affairs
Pharmaceutics
Drug Development
Regulatory Affairs
Pharmacovigilance
Cro
Clinical Data Management
Regulatory Submissions
Clinical Operations
Fda
Medical Writing
U.s. Food and Drug Administration
Electronic Data Capture
Standard Operating Procedure
Good Clinical Practice
Clinical Trial Management System
Cro Management