Sr Clinical Research Assistant PD

Summary Under general supervision, but following established policies and procedures, performs scientific investigative research in areas related to research participant care. Research literature in the field, participates in the design of experimental protocols and develops new procedures to carry out established research objectives. Interviews research participants to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in the qualitative/quantitative analyses of data. May assist in writing presentations and papers for publication based on the research performed. May perform PSG and take vital signs during research‑based monitoring tests. May also perform saliva/blood spinning and shipment of tissue samples as required by protocol. Responsibilities In collaboration with the research investigator, participates in the design of experimental protocols to achieve the scientific objectives of the research project. Develops research methodologies within the parameters of experimental protocols and research objectives to allow quantitative and qualitative evaluation and interpretation of data obtained. Establishes and maintains study record for each participant. Interviews research participant and/or family to explain the nature of the study, eliciting cooperation and gathering information to complete the study questionnaire. Facilitates obtaining informed consent. May assist to schedule research participant appointments and make calls to research participants to complete documentation. Regularly monitors adherence to protocol and takes action to ensure research protocols are conducted correctly. Collects and organizes research participant data into appropriate format to facilitate data entry. Creates, modifies as appropriate and maintains study database to meet needs for the project. Gathers, tabulates, graphs, develops explanatory charts, and analyzes data using statistical methodology. Performs computer‑assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross‑tabulation and the like. Prepares and maintains related graphs and charts or results of data gathered. Participates in quantitative/qualitative analyses of resultant information. Provides functional guidance and supervision to subordinate research staff assigned to the project to clarify protocol, resolve issues, ensure adherence to research protocol procedures and assist in developing their technical and professional skills. Participates in the interpretation of results through conferences with the principal investigator and other research professionals involved in the study to review data compared to hypothesis and research methodology in instances of inexplicable data. May make recommendations for modification of research protocol based upon initial findings. May assist in writing presentations and papers for publications based on research performed. Regularly reviews relevant literature to better understand the project. Maintains and enhances professional expertise through educational opportunities and participation in related teams and conferences. May perform research‑based physiological recording, saliva or blood spinning, and shipping of saliva or blood and tissue products, in accordance with protocol specifications. Minimum Qualifications Bachelor’s Degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems. Experience in sleep research a plus. Two to three years progressively more responsible and related experience in the research field. Experience should demonstrate effective working knowledge of statistics, computer programming, and research methodology and an in‑depth knowledge of the scientific field in which research is being conducted. Provides functional training and guidance to subordinate research staff assigned to the project. Salary and Employment Pay Range: $23.11 - $38.16 Location Bradley Hospital - 1011 Veterans Memorial Pkwy, East Providence, Rhode Island 02915 Work Type Varies for PD work Work Shift Day; Daily Hours: Per Diem – As required Driving Required No EEO Statement Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment. #J-18808-Ljbffr EPBH Emma Pendleton Bradley Hospital