Clinical Research Assistant-Sunnyvale, CA
ProTrials Research, Inc. - Sunnyvale, CA

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The Clinical Research Assistant (CR Assistant) supports Clinical Research team members. The CR Assistant shall work well under pressure, and meet multiple and sometimes competing deadlines. The CR Assistant shall at all times demonstrate cooperative and professional behavior with colleagues, clients and supervisors in compliance with the Standards of Professional Conduct. The CR Assistant will support and provide administrative assistance by performing all or some of the tasks listed below: Essential DutiesObtains, reviews, processes, and tracks study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.)Maintains and disseminates basic study tracking information including, but not limited to: Visit ReportsRegulatory Documents Site Contact ListsTeam Contact ListsVendor ListsBudget DisbursementsManages and tracks Investigational Product supplies for study centers: receives and prepares requests, ships and returns Investigational Product suppliesPrepares, ships and manages inventory of study related suppliesGathers investigator and site information (addresses, phone numbers, fax numbers, personnel names and email addresses, etc.)Assists in preparing materials for investigators meetings, monitor workshops, and study manualsTakes minutes of meetings with project teams, sponsors, or vendors as approved by PMCommunicates effectively with members of the ProTrials project teams, interfacing directly with sponsor as directed by PM.Other duties as assigned.Qualifications: Minimum Preferred: RN and/or 4-year degree, preferably in a scientific or health care discipline, or equivalent combination of education and experience. Successful completion of the ProTrials interview process, including interviews, reference checks, etc. Minimum 1 year of experience with clinical trials preferred.Skills & Abilities Required: Attention to detailExcellent organizational skillsEffective communication and interpersonal skills Ability to efficiently perform multiple tasks and manage changing prioritiesAbility to identify and solve logistical problemsAbility to work effectively on a diverse team Ability to read and understand regulatory documents and Standard Operating ProceduresDemonstrates proficiency in Microsoft Word and Excel Takes direction well

Keywords: Clinical Trials Management Certification, ACRP

ProTrials Research, Inc. - 23 months ago - save job
About this company
ProTrials, founded in 1996, is a clinical operations firm headquartered in Mountain View, California. The Company provides clinical research...