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#40192: Director / Program Manager |
| Post Date: |
2010-08-10 |
| Location: |
West Coast / Southwest |
| Salary: |
90K - 125K |
| Benefits: |
Bonus, options |
| Startup: |
No |
| Description: |
Recognized as an expert and resource in clinical study conduct for domestic clinical trials. Considered a mentor to junior CRAs. Leads other CRAs to maintain consistent trial management across sites. In addition, will prepare clinical protocols and reports; and clinical sections of EMEA regulatory submissions.
Individual responsible for successfully developing and executing all clinical study activities for the interventional opportunity (peripheral and aortic). Writing effective protocols for clinical studies in accordance with FDA and other regulatory authorities. This position also requires investigational center management and clinical program implementation. This person must assist R & D team and project leaders in the design and development of products in accordance with quality standards and customer requirements/requests.
BS in Life Sciences, biomedical engineering, nursing, or other technical dispute. 10 years experience in the medical device or related industry, along with 5 years exp. in designing and managing multiple multi-centered clinical trials and data collection with Class III devices.
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