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Clinical Study Manager Job
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| Employer Name: BiotechCrossing |
SpiderID: 2203758 |
| Location: Saint Louis, Missouri |
Date Posted: 4/25/2008 |
| Wage: |
Category: Biotech |
| Job Code: |
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Job Description:
You will manage one or more clinical research project teams which may include internal personnel or external vendors. The incumbent will be responsible for financial and operational performance of assigned projects to ensure that project/program milestones and objectives are met. This position supports the development of the project/program scope of work, project costs, timelines, metrics and deliverables.The successful candidate will have a bachelors degree, preferably in a scientific discipline. Minimum four years of clinical research experience and two years of clinical study management experience in a pharmaceutical/biotechnology company, CRO, or clinical trials research environment. Minimum of one year supervisory experience required, two years preferred. You must have the ability to travel as needed (estimated at 25% to 30%). If you have detailed knowledge of FDA/GCP/ICH clinical requirements for clinical trial conduct, the ability to exercise independent judgment and creativity in developing methods, techniques and evaluation criteria for obtaining results this may be the position for you. We are seeking a self-motivated individual with the ability to be effective with minimum supervision.
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Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:
Contact Information:
| Contact Name: - |
Company Type: Employer |
| Company: BiotechCrossing |
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| City: Pasadena |
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| State: California |
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| Zip: |
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Web Site: http://www.biotechcrossing.com
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