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Thomas Jefferson Univ Clinical Research Coordinator II in Philadelphia, Pennsylvania

PRIMARY FUNCTION:The Clinical Research Coordinator III runs portions of clinical trials, assists with orientation and training, obtains signatures for informed consent, manages data, completes expectancy reports, monitors visit preparation, submits low institutional risk trials and tracks TJU IRB submission and approvals..and.nbsp;ESSENTIAL FUNCTIONS:.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP)..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Trains and supervises research staff on the proper procedures for conducting a clinical trial per GCP..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies as required to ensure compliance..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Maintains accurate subject log, tracks expenses, submits appropriate documentation to Grant Administrator for payment due for visits..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Performs quality control assessments, ensuring clinical trial data is collected and stored per GCP..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Organizes and maintains documentation of patient data..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Designs electronic capture databases as needed and manages collected data..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Interacts with co-workers, visitors, and other staff consistent with the iSCORE values of Jefferson._________________________________________________________________________OTHER FUNCTIONS AND COMPETENCIES:.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Performs additional administrative duties that will include participation in weekly research team meetings; secures storage and back-up of data; electronic back-up storage of operations research models as they are progressively formulated;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Maintains Institutional Review Board communications, contract agreements, and expense files..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Attends regular meetings involving the entire research team. During these research team meetings, the Research Coordinator offers expertise where appropriate and documents the discussions between investigators and other research team members..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Performs other duties as assigned.EDUCATIONAL/TRAINING REQUIREMENTS:Bachelors DegreeMasters DegreeNo Degree.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; (See Below for Corresponding Experience)_________________________________________________________________________CERTIFICATES, LICENSES, AND REGISTRATION:N/A_________________________________________________________________________EXPERIENCE REQUIREMENTS:If Bachelors Degree: 2 years Clinical Research ExperienceIf Masters Degree: 1 Year Clinical Research ExperienceIf No Degree: 8 Years Clinical Research ExperienceIf No degree and SOCRA/ACRP Certificate: 6 Years Clinical Research Experience________________________________________________________________________ADDITIONAL INFORMATION:.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Confidentiality: Knowledge of practices and policies governing disclosure of information about the organization, its business activities, and employees, ability to apply this knowledge appropriately to diverse situations..and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp;.and.nbsp; - Critical Thinking and Process Management: Knowledge of business process improvement tools and techniques and ability to understand, monito

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