Regional Clinical Research Associate
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Company: Prestige Scientific
Contact Name: Joe Freddolino
- Email your resume (Click Here)
- Mail To:
1 Maple Street
Milford 01757
- Phone: 508-422-9322
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- Job ID:
- Date:06/27/2008
- Location:Home Based
- State:Not Listed
- Degree:B.S./B.A.
- Current Professional Level:Experienced Staff Level
- Salary:Not Specified Why?
- Job Types:
-
Clinical Research Associate
Job Description
Regional CRA (Midwest & Northwest U.S.) Conduct site selection, initiation, monitoring and close out visits at assigned clinical trial centers in accordance with International Conference on Harmonization Good Clinical Practice (ICH GCP) Guidelines.
SPECIFIC DUTIES: Attend Orientation meeting. Attend Investigator meetings where applicable. Conduct and report on Site Qualification Visits. Conduct and report on Site Initiation Visits. Conduct and report on Routine Monitoring Visits in accordance with frequency/scheduling requirements. Conduct regular follow up with Investigator Sites in accordance with site management requirements. Anticipate, identify, communicate and resolve issues at assigned Investigator Sites Resolve all Data Queries as required. Conduct and report on Site Closure Visits. Provide regular project updates to the Project Manager/Director or designee. Attend Project Team meetings and teleconferences as required.
REQUIREMENTS: Health professional background. Minimum 1-year experience as a Clinical Research Associate or 2 years as a Clinical Research Coordinator. Minimum 8-10 on-site visit days. Competency in all facets of clinical trial monitoring. Oncology and/or transplantation and/or HIV experience an asset. Computer proficiency (Word and Excel). Knowledge of Lotus notes is an asset. Excellent verbal and communication skills. Professional image and ability to travel at least 50% of the time. Ability to independently plan and prioritize own work schedule. Bilingualism an asset (French and English).
Additional Comments: This is a home-based position.
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