CRA - Biotech Resume Search
CRA - Biotech Resume Search
Home
Contacting Us
F. A. Q.
Links
Log In
Scam Awareness
 
 
Job Seekers
Browse Jobs
Search Jobs
Post a Resume
Modify Resume
Delete Resume
Job Alerts
 
Employers
Browse Resumes
Search Resumes
Post a Job
Modify Job Ad
Delete Job Ad
 
Resources
Employment Directory

CRA Resume


Desired Industry: Biotech SpiderID: 16817
Desired Job Location: Providence, Rhode Island Date Posted: 11/5/2007
Type of Position: Full-Time Permanent Availability Date: 11/15/07
Desired Wage: $75,000
U.S. Work Authorization: Yes
Job Level: Experienced with over 2 years experience Willing to Travel: Yes, 50-75%
Highest Degree Attained: Bachelors Willing to Relocate: Yes


Objective:
To obtain a senior clinical research associate position in a pharmaceutical company or contract research organization.


Experience:
Pfizer Animal Health (Groton, CT and Richland, MI) 1999-2007
Veterinary Clinical Research Associate

•Act as liaison between individual study sites and Sponsor.
•Prepare, collect and track protocols, amendments, deviations, regulatory documents, data capture forms, final study report and assist in the planning of new studies.
•Assure that study files are maintained and required documentation is collected.
•Assist in the selection of Investigators and inspection of study sites to assess adequacy of conducting studies.
•Assist in the budget and grant tracking process.
•Review data capture forms to ensure clarity, legibility, and completeness of entries and compliance with the protocol.
•Assure, on an ongoing basis, that study sites have adequate clinical supplies and test articles.
•Perform data verification and resolves queries.
•Maintain a sufficient understanding of FDA/USDA/VICH regulations, the disease process under study, and mechanism of drug action.
•Create a data review plan to assure that the data handling and entry process is tracked and monitored for timeliness and accuracy.
•Review Investigator invoices for accuracy and completeness.
•Monitor individual study sites by regularly scheduled visits and/or by telephone; resolve issues while proactively minimizing future issues.
•Review source data at investigational sites to validate the data entered into data capture forms, and assure the proper accounting for test articles.
•Assure compliance of the Investigator with the protocol, informed consent, and test article storage requirements.
•Plan and participate in Investigator training meetings and assure that all personnel at sites are fully aware of their responsibilities in the study.



Education:
University of Phoenix
M.B.A.-Global Marketing expected 2008

University of Rhode Island
B.S.-Animal and Veterinary Science 1999
Minor-Philosophy and Ethics


Candidate Contact Information:
Name: Stephanie Tarnacki
Street:    - Phone: 401-480-0135
City:    - Fax:    -
State:    -
Zip: 02816
Web Site:


    



© 2003 CC Marketing and Classified Systems
Privacy Policy | CC Marketing Sites | Site Map