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consent forms and master subject logs. File all appropriate correspondence. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform
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educational background in medicine and/or scientific field (biological sciences, social sciences, etc.) Strong oral and written communication skills Excellent attention to detail Proficiency in using computers
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Microsoft Office. Knowledge of medical terminology. CERTIFICATIONS & LICENSES: Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. PHYSICAL
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