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Search By State | Search By Job Type |
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5 Found |
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Job Title |
Post Date |
Company Name |
Job Location |
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Regional CRA - Home Based
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6/15/2008
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Sterling Life Sciences
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Missouri,
Massachusetts-
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1) Track screening and enrollment as well as identify issues to be addressed globally
2) Confirm (independently) that site regulatory documents match TMF
3) Act as an expert on subject matter for junior staff and mentor junior colleagues
4) Contact sites on a consistent basis ...
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Clinical Research Associates
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6/15/2008
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Sterling Life Sciences
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Home Based,
New-Jersey-
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1) Monitor pre-study, initiation, routine and closeout visits at investigator sites for GCP compliance as per company SOPs and client guidelines
2) Generate study specific documentation, including monitoring trip reports, telephone contact reports, site correspondence and expen ...
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Medical Director - Sr. Medical Director
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5/25/2008
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Acadia Pharmaceuticals
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San Diego,
California-
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While working as a member of the Development Team, the Medical Director/Sr. Medical Director, CNS, will design and finalize protocols and other trial documents for Phase I-II-III clinical trials; identify and recruit clinical trial sites and investigators and manage these relati ...
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Manager, Clinical Trials Material
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5/25/2008
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Acadia Pharmaceuticals
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San Diego,
California-
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This position is responsible for the management of Clinical Trials Material (CTM) in support of Global R&D Clinical Trials and other supportive research or development needs. Responsible for determining CTM requirements through protocol review, ensuring label compliance with app ...
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Clinical Project Assistant
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5/25/2008
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Acadia Pharmaceuticals
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San Diego,
California-
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* Procuring and reviewing site regulatory documents
* Maintaining study-specific tracking systems
* Processing all forms concerning data collection, payments, and other materials regarding clinical trials
* Managing active study files and preparing key documents ...
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