Study Coordinator Pre-Clinical Studues

Designs, plans, implements and coordinates pre-clinical studies according to SOP and GLP (God Laboratory Practices). These duties include preparation of study protocols, coordination with all necessary departments, ensure proper documentation, assist in finalizing data and preparing study files for achival for in house and contracted studies. Responsible for study planning meetings. Assist in finalization of studies including preparation of reports, figures, appendices and tables including editing/formating of various documents. Editing and formating of various regulatory documents.
Required skills: At least intermediate level word processing skills MS Word and Excel. Excellent verbal and written communication skills. Familiarity with GLP guidelines, toxicology and/or pharmacology in vivo studies. Must be organized and able to handle several tasks/projects at the same time. Experience with electronic data capture systems is helpful. Science background is a plus.

Job Title: Study Coordinator Pre-Clinical Studues
Primary Skills: SOP's GLP; Toxicology; Pharmacology in vivo studies
Job Industry: Biotech/Pharmaceutical
Vacancies: 1
Job City: Palo Alto
Job Metro Area: Palo Alto
Job State: CA
Job Country: US
Salary: DOE
Hours per Week: 40
Start Date: ASAP
Job Duration: 3 - 6 months
Detailed Job Duration: 4 months
Degree Type: BS
Degree Area: Life Science
Experience Minimum: 1 Years
Certificates/Licenses:

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