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Clinical Research Associate (CRA)
| Details |
Country: USA
Location: IL Deerfield
Total applied: 2
Job Type: Temporary / Contract / Project
Job Status: Full Time
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Clinical Research Associate (CRA)
3-5 years of coordinating or monitoring experience of Phase I-III studies. Thorough understanding of drug development process including protocol compliance & study documentation requirements, familiar with 21 CFR and ICH GCP. Proficiency in Microsoft Office (especially Word and Excel), excellent verbal and nonverbal communication skills. This person will work in Research Quality Assurance assisting with audit responses and will act as primary liaison with clinical and preclinical supply vendors. Quality Assurance Audit Database (QAAD) experience preferred. All initial meetings will be phone screen.
Job Title: Clinical Research Associate (CRA)
Primary Skills: 21 CFR Part 11; Clinical; Microsoft Office; QAAD
Job Industry: Biotech/Pharmaceutical
Vacancies: 1
Job City: Deerfield
Job Metro Area: Deerfield
Job State: IL
Job Country: US
Salary: DOE
Hours per Week: 40
Start Date: 08/28/2006
Job Duration: 3 - 6 months
Detailed Job Duration: 4 months
Degree Type: BS
Degree Area: Clinical or Related
Experience Minimum: 3 Years
Certificates/Licenses:
To submit a resume for this position, you must place PR60031/MB/30915EDHE in the subject line of your e-mail. Send your resumes to:
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