PROJECT ADMINISTRATOR TECHNICAL RESOURCES INT'L

Bethesda, MD Job Details Full-time 3 hours ago Qualifications Database systems Productivity software Clinical quality assurance standards Systems analysis FDA regulations

Full Job Description Job Description:

Assists on project management ad-hoc activities, produces reports, assists on editing of project and trial documents, etc. Generates level of effort reports and assists in monitoring project status Drafts and submits project progress reports Coordinates team conference calls, generates and distributes meeting minutes from internal/client/vendor meetings as applicable Prepares, revises, analyzes and reconciles project documents, including standard operating procedures (SOPs), project management plan, risk management plan, training plan, metrics and findings reports, etc., within specified timelines Assists with clarification and resolution of findings from quality assurance audits Maintains assigned data points within project tracking systems according to the established conventions within specified times, including entry of findings Provides ad hoc support as needed

Job Requirements:

Excellent oral and written communication skills and interpersonal skills Detail-oriented and able to multi-task/prioritize well, with proven ability to handle multiple tasks efficiently and effectively Strong working knowledge of Microsoft office and ability to obtain knowledge and master all clinical trial database systems and technical tools; experience with AI tools a plus Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency Flexibility to reprioritize workload to meet changing project timelines Knowledge of FDA clinical trial guidelines and regulations Clinical research experience preferred This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely.