Yale University
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Research Associate 2
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Yale University Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community- eligible for opportunities through the New Haven Hiring Initiative or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Salary Range : $65,000.00 - $101,000.00 Overview : Participates in the design, administration, and monitoring, primarily of pediatric and adolescent clinical trials, with a main focus on type 1 diabetes. Reporting to the TrialNet principal investigator, independently, and in collaboration with the research team, manage scheduling and follow up with families involved in research studies in addition to performing other study related procedures. Participate in the recruitment of study participants for research protocols, evaluating the participants for inclusion in protocols; based on knowledge of protocol and study requirements, coordinate operation of study protocols with the investigators and other members of the study team define the parameters and eligibility criteria for study enrollment in order to guide the clinical team in identifying viable research candidates; obtain informed consent; responsible for the creation maintenance of accurate data records, report adverse events to the study and clinical teams; manage study supply provision; educate participants in the use of study devices based on the knowledge and understanding of these devices; assist researchers in preparation of manuscripts; participate actively in research meetings, presenting information and updates as required; participate in conference calls with the coordinating center regarding study conduct; consult with families and with research coordinating centers using knowledge, understanding ; provide feedback to coordinating center for protocol development and revision; interact with both internal and external contacts regarding clinical trials; adheres to quality control measures to ensure accurate collection and processing of data. Due to the multiple study dynamics, you will be required to meet patients at different hospital locations Required Skills And Abilities Excellent written and verbal communication skills. Strong interpersonal skills to allow for successful relationships with patients. Strong organizational skills and attention to detail, with the ability to multitask, prioritize tasks, and manage time effectively. Demonstrated ability to work both independently and as part of a multidisciplinary team. Proficiency in Microsoft Office Suite. Must have CT motor vehicle license and own vehicle to travel to different hospitals. Preferred Skills And Abilities Bilingual in Spanish. Prior experience in clinical research or clinical trials with demonstrated ability to assess inclusion/exclusion criteria, familiarity with the consenting process. Experience with data analysis. Demonstrated experience with use of electronic medical records for research including the ability to screen potential participants for eligibility as well as extract data needed for study purposes. Demonstrated experience in and ability to critically evaluate patient information to meet eligibility requirements. Familiarity with IRB processes including the ability to develop and attain approval HIC/IRB approval of proposed trials and maintenance of ethical approvals/certification. Principal Responsibilities Carries out research within the scope of the established study protocol. Adheres to all human subjects regulations as defined by Yale University and the federal government that pertain to research studies. Develops criteria for admission of study subjects based on goals and objectives of project. Determines potential sources of funding and prospective partnerships. Evaluates feasibility of accepting potential projects through analysis of staffing needs, resource requirements, financial costs, and current planned capacity of group. Negotiates contracts and/or changes with funder. Develops original HIC/IRB submissions. Based on knowledge of science and research goals, collaborates with PIs on major revisions and contributes to scientific protocols. Plans and implements changes. Develops forms, questionnaires and the application of research techniques; writes procedures manuals for data collection and coding. Responsible for the documentation and transmission of study data. Ensures that report forms are accurately documented and completed in a timely manner at each site location. Works independently to develop manage and organize multi site studies. Serves as primary coordinator between University, non-Yale collaborators, pharmaceutical companies, HIC, IRB and funding sources. Performs descriptive and multivariate statistical analyses of data, using computer software. Designs and implements quality control measures to ensure accurate collection and processing of data. Contributes in-depth, original thought and relevance to written reports and to the writing of abstracts and manuscripts. Yale University is an Equal Opportunity Employer and welcomes applications from diverse candidates. Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).
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Research Associate 2
role at
Yale University Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community- eligible for opportunities through the New Haven Hiring Initiative or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Salary Range : $65,000.00 - $101,000.00 Overview : Participates in the design, administration, and monitoring, primarily of pediatric and adolescent clinical trials, with a main focus on type 1 diabetes. Reporting to the TrialNet principal investigator, independently, and in collaboration with the research team, manage scheduling and follow up with families involved in research studies in addition to performing other study related procedures. Participate in the recruitment of study participants for research protocols, evaluating the participants for inclusion in protocols; based on knowledge of protocol and study requirements, coordinate operation of study protocols with the investigators and other members of the study team define the parameters and eligibility criteria for study enrollment in order to guide the clinical team in identifying viable research candidates; obtain informed consent; responsible for the creation maintenance of accurate data records, report adverse events to the study and clinical teams; manage study supply provision; educate participants in the use of study devices based on the knowledge and understanding of these devices; assist researchers in preparation of manuscripts; participate actively in research meetings, presenting information and updates as required; participate in conference calls with the coordinating center regarding study conduct; consult with families and with research coordinating centers using knowledge, understanding ; provide feedback to coordinating center for protocol development and revision; interact with both internal and external contacts regarding clinical trials; adheres to quality control measures to ensure accurate collection and processing of data. Due to the multiple study dynamics, you will be required to meet patients at different hospital locations Required Skills And Abilities Excellent written and verbal communication skills. Strong interpersonal skills to allow for successful relationships with patients. Strong organizational skills and attention to detail, with the ability to multitask, prioritize tasks, and manage time effectively. Demonstrated ability to work both independently and as part of a multidisciplinary team. Proficiency in Microsoft Office Suite. Must have CT motor vehicle license and own vehicle to travel to different hospitals. Preferred Skills And Abilities Bilingual in Spanish. Prior experience in clinical research or clinical trials with demonstrated ability to assess inclusion/exclusion criteria, familiarity with the consenting process. Experience with data analysis. Demonstrated experience with use of electronic medical records for research including the ability to screen potential participants for eligibility as well as extract data needed for study purposes. Demonstrated experience in and ability to critically evaluate patient information to meet eligibility requirements. Familiarity with IRB processes including the ability to develop and attain approval HIC/IRB approval of proposed trials and maintenance of ethical approvals/certification. Principal Responsibilities Carries out research within the scope of the established study protocol. Adheres to all human subjects regulations as defined by Yale University and the federal government that pertain to research studies. Develops criteria for admission of study subjects based on goals and objectives of project. Determines potential sources of funding and prospective partnerships. Evaluates feasibility of accepting potential projects through analysis of staffing needs, resource requirements, financial costs, and current planned capacity of group. Negotiates contracts and/or changes with funder. Develops original HIC/IRB submissions. Based on knowledge of science and research goals, collaborates with PIs on major revisions and contributes to scientific protocols. Plans and implements changes. Develops forms, questionnaires and the application of research techniques; writes procedures manuals for data collection and coding. Responsible for the documentation and transmission of study data. Ensures that report forms are accurately documented and completed in a timely manner at each site location. Works independently to develop manage and organize multi site studies. Serves as primary coordinator between University, non-Yale collaborators, pharmaceutical companies, HIC, IRB and funding sources. Performs descriptive and multivariate statistical analyses of data, using computer software. Designs and implements quality control measures to ensure accurate collection and processing of data. Contributes in-depth, original thought and relevance to written reports and to the writing of abstracts and manuscripts. Yale University is an Equal Opportunity Employer and welcomes applications from diverse candidates. Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).
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