Research Coordinator
4.
1 Seattle, WA Seattle, WA Temporary Part-time Temporary Part-time $5,000 - $5,600 a month $5,000 - $5,600 a month 13 hours ago 13 hours ago 13 hours ago Research Coordinator (hourly for 90 days, then PT):
Apply directly at:
https:
//uwhires.
admin.
washington.
edu/eng/candidates/default.
cfm?szCategory=jobprofile&szOrderID=228965&szCandidateID=0&szReturnToSearch=1 Research coordinator will support the development of research materials and implementation of research activities under the direction of the Principal Investigator.
This includes the coordination and tracking of research activities across research sites; assisting in the development of study tools and research protocols; completing and monitoring human subject applications, modifications, and renewals; documenting completion of HIPPA training, coordination with UW fiscal and purchasing staff; assisting with research training; conducting recruitment, randomization, tracking, and timely data collection and entry; assisting with data analysis, project reports, and dissemination of research results.
The position requires knowledge of clinical intervention research and randomized trials, experience in health-related research and/or web-based intervention delivery, collection of quantitative, qualitative, and biological data, strong organizational and interpersonal skills, familiarity with computer software programs necessary for successful the implementation and flow of research processes including study recruitment, enrollment, randomization, oversight of research regulatory requirements, data management and preliminary data analyses and reports.
Study phase design, research coordination & study implementation Coordinate, monitor, and report research site progress, including study recruitment and randomization, coordination with research sites, consent process, access and storage of relevant medical record information, intervention schedules and session completions, mailings and data collection processes, and general management of study activities.
Support regulatory compliance and reporting (Human Subject, HIPPA, recruitment & enrollment).
Prepare Human Subject applications, modifications, consent forms, and progress reports for the institutional review board and funding agency as directed by PI.
Develop working relationships with designated study staff across recruitment sites.
Coordinate communication and activities among research team members, routinely keep the PI informed of the SPSM Intervention schedule, recruitment progress, intervention calls completed, and related research concerns.
Coordinate with the nurse interventionist to ensure intervention procedures are initiated and completed on time.
Following established protocols, contact potential study participants, screen for eligibility, describe study activities, obtain informed consent, and enroll and follow-up with eligible individuals.
Design and maintain databases to track subject participation (enrollment, randomization, pacing of intervention), weekly intervention calls, data collection and missing data, securing medical records, health histories, and other data-related tasks.
Track receipt of biomarker data.
Monitor and download StepWatchTM data returned by mail.
Troubleshoot implementation-related issues (e.
g.
, access and function of web-based intervention modules; preparation/tracking of mailed materials; and related duties including filing, copying, and data entry.
Organize and oversee exit of participants from the study (e.
g.
, write checks/send gift cards, thank you letters; create/send Study Newsletters).
Analyzing data and Presenting Research Results Organize, enter, verify, backup, and store all incoming data; perform routine assessment of data and computer management systems.
Routinely analyze and summarize preliminary quantitative study findings for the research team, including descriptive analyses, summary reports with tables/figures; create interim reports as requested by PI.
Order materials and scientific supplies for research and intervention implementation.
Support PI and research staff in generating reports for the funding agency (NIH).
Prepare for and participate in research team meetings.
Contribute to interim reports and the development of research manuscripts and grants.
As necessary, train and monitor student assistant to support the use of software (REDCap) to track recruitment, consents, intervention enrollment and progress Prepare data and conduct preliminary coding of responses to exit interviews for qualitative analysis.
n producing materials for and provide support for study-related trainings, as needed.
Requirements:
Bachelor's or graduate degree (preferred) in health or related behavioral or social sciences.
Two-three or more years of experience as a research coordinator or equivalent for adult clinical trials.
Experience with 1) quantitative research techniques, randomized clinical trial designs, behavioral intervention, subject randomization, and coordinating collection of biological samples; 2) in organizing and coding qualitative data to evaluate intervention impact; 3) Experience with research methods used to evaluate intervention feasibility/acceptability delivered by diverse means (in person, telephone, small group and/or computer interface) Strong computer skills; experience with research-related software such as (or similar to) REDCap, SPSS, ZOOM, PowerPoint, and EXCEL.
Demonstrated excellence in organizational skills, attention to detail, time management, ability to prioritize tasks, and meet deadlines.
Excellent decisional skills and proficiency in cross-cultural communication.
Experience in meeting funding agency requirements and related research milestones.
Skills, knowledge, and/or experience working with health professionals, nurses, and students, and in the development and/or implementation of training programs for research staff.
Ability to work in-person onsite at the UW-Seattle locations 5 days/week.
Flexibility in work schedule that may involve late afternoon, early morning, or evening work hours Job Types:
Temporary, Part-time Pay:
$5,000.
00 - $5,600.
00 per month Expected hours:
15 - 20 per week Experience level:
2 years Medical specialties:
Cardiology Schedule:
4 hour shift Monday to Friday Education:
Master's (Required)
Experience:
research coordination:
1 year (Required) Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
1 Seattle, WA Seattle, WA Temporary Part-time Temporary Part-time $5,000 - $5,600 a month $5,000 - $5,600 a month 13 hours ago 13 hours ago 13 hours ago Research Coordinator (hourly for 90 days, then PT):
Apply directly at:
https:
//uwhires.
admin.
washington.
edu/eng/candidates/default.
cfm?szCategory=jobprofile&szOrderID=228965&szCandidateID=0&szReturnToSearch=1 Research coordinator will support the development of research materials and implementation of research activities under the direction of the Principal Investigator.
This includes the coordination and tracking of research activities across research sites; assisting in the development of study tools and research protocols; completing and monitoring human subject applications, modifications, and renewals; documenting completion of HIPPA training, coordination with UW fiscal and purchasing staff; assisting with research training; conducting recruitment, randomization, tracking, and timely data collection and entry; assisting with data analysis, project reports, and dissemination of research results.
The position requires knowledge of clinical intervention research and randomized trials, experience in health-related research and/or web-based intervention delivery, collection of quantitative, qualitative, and biological data, strong organizational and interpersonal skills, familiarity with computer software programs necessary for successful the implementation and flow of research processes including study recruitment, enrollment, randomization, oversight of research regulatory requirements, data management and preliminary data analyses and reports.
Study phase design, research coordination & study implementation Coordinate, monitor, and report research site progress, including study recruitment and randomization, coordination with research sites, consent process, access and storage of relevant medical record information, intervention schedules and session completions, mailings and data collection processes, and general management of study activities.
Support regulatory compliance and reporting (Human Subject, HIPPA, recruitment & enrollment).
Prepare Human Subject applications, modifications, consent forms, and progress reports for the institutional review board and funding agency as directed by PI.
Develop working relationships with designated study staff across recruitment sites.
Coordinate communication and activities among research team members, routinely keep the PI informed of the SPSM Intervention schedule, recruitment progress, intervention calls completed, and related research concerns.
Coordinate with the nurse interventionist to ensure intervention procedures are initiated and completed on time.
Following established protocols, contact potential study participants, screen for eligibility, describe study activities, obtain informed consent, and enroll and follow-up with eligible individuals.
Design and maintain databases to track subject participation (enrollment, randomization, pacing of intervention), weekly intervention calls, data collection and missing data, securing medical records, health histories, and other data-related tasks.
Track receipt of biomarker data.
Monitor and download StepWatchTM data returned by mail.
Troubleshoot implementation-related issues (e.
g.
, access and function of web-based intervention modules; preparation/tracking of mailed materials; and related duties including filing, copying, and data entry.
Organize and oversee exit of participants from the study (e.
g.
, write checks/send gift cards, thank you letters; create/send Study Newsletters).
Analyzing data and Presenting Research Results Organize, enter, verify, backup, and store all incoming data; perform routine assessment of data and computer management systems.
Routinely analyze and summarize preliminary quantitative study findings for the research team, including descriptive analyses, summary reports with tables/figures; create interim reports as requested by PI.
Order materials and scientific supplies for research and intervention implementation.
Support PI and research staff in generating reports for the funding agency (NIH).
Prepare for and participate in research team meetings.
Contribute to interim reports and the development of research manuscripts and grants.
As necessary, train and monitor student assistant to support the use of software (REDCap) to track recruitment, consents, intervention enrollment and progress Prepare data and conduct preliminary coding of responses to exit interviews for qualitative analysis.
n producing materials for and provide support for study-related trainings, as needed.
Requirements:
Bachelor's or graduate degree (preferred) in health or related behavioral or social sciences.
Two-three or more years of experience as a research coordinator or equivalent for adult clinical trials.
Experience with 1) quantitative research techniques, randomized clinical trial designs, behavioral intervention, subject randomization, and coordinating collection of biological samples; 2) in organizing and coding qualitative data to evaluate intervention impact; 3) Experience with research methods used to evaluate intervention feasibility/acceptability delivered by diverse means (in person, telephone, small group and/or computer interface) Strong computer skills; experience with research-related software such as (or similar to) REDCap, SPSS, ZOOM, PowerPoint, and EXCEL.
Demonstrated excellence in organizational skills, attention to detail, time management, ability to prioritize tasks, and meet deadlines.
Excellent decisional skills and proficiency in cross-cultural communication.
Experience in meeting funding agency requirements and related research milestones.
Skills, knowledge, and/or experience working with health professionals, nurses, and students, and in the development and/or implementation of training programs for research staff.
Ability to work in-person onsite at the UW-Seattle locations 5 days/week.
Flexibility in work schedule that may involve late afternoon, early morning, or evening work hours Job Types:
Temporary, Part-time Pay:
$5,000.
00 - $5,600.
00 per month Expected hours:
15 - 20 per week Experience level:
2 years Medical specialties:
Cardiology Schedule:
4 hour shift Monday to Friday Education:
Master's (Required)
Experience:
research coordination:
1 year (Required) Work Location:
In person.
Estimated Salary: $20 to $28 per hour based on qualifications.
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