Clinical Project Associate
The position entails work under general supervision for routine tasks and with detailed instructions on new assignments. Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools. Reviewing and participating in the quality assurance of data or documents. Arranges meeting logistics. Drafts meeting agendas and assists in preparing meeting minutes. (Interacts with other departments, as directed, to complete assigned tasks). Assist in review and filing of clinical trial documents into electronic trial master file. Assists with development of clinical trial documents and standard forms. Orders and maintains inventory of clinical supplies.. Assists with development of documents for site binders. Serves as CRA back up providing verbal and written communication with study personnel. Under close supervision reviews and participates in the quality assurance of data or documents. May assist with monitoring visits under the direct supervision of senior staff. Travel may be required. Excellent verbal and written communication skills and interpersonal skills are required. Must be familiar with Word, PowerPoint, and Excel. Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is a plus. Must be able to work both independently and as part of a team.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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