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*THIS IS NOT A VIRTUAL POSITION, YOU MUST LIVE WITHIN OR BE WILLING TO RELOCATE WITHIN A COMMUTABLE DISTANCE OF THE DUTY LOCATION***
This is a term appointment not to exceed 4 years. Term appointments are non-status, nonpermanent appointments of limited duration of more than 1 year, but not more than 4 years and are subject to a 1 year trial period. Should the need warrant, term appointments may be extended without further competition up to a maximum of the 4 year limitation. The appointment to a term position does not confer eligibility for promotion, reassignment, or transfer to other positions or the ability to be non-competitively converted to permanent employment.
Major duties and responsibilities include but not limited to:
- Coordinating assigned research studies and projects by implementing study protocols, managing timelines, supporting patient/participant recruitment and interactions, overseeing data and biospecimen collection, completing data entry, and communicating with collaborators and project personnel
- Ensuring research activities comply with approved protocols, regulatory requirements, scientific standards, and quality expectations while maintaining accurate study records, databases, regulatory documentation, and research files
- Managing and improving research databases and data repositories in collaboration with the PI, biostatistics/statistics teams, and research staff to support data storage, organization, analysis, and integrity
- Performing data quality assurance activities by reviewing data for accuracy, completeness, inconsistencies, outliers, missing information, and protocol deviations while recommending corrective actions
- Developing and implementing quality improvement processes to ensure consistent research procedures and reliable, scientifically valid data collection
- Supporting scientific dissemination efforts through preparation of manuscripts, abstracts, reports, presentations, and other research materials while providing data summaries, interpretations, and contributions aligned with authorship standards
- Conducting literature reviews and summarizing relevant scientific findings to support research objectives, study development, and ongoing project activities
- Providing supervision, training, and coordination of research assistants and support personnel by assigning tasks, monitoring progress, and ensuring adherence to study protocols and quality standards
- Coordinating administrative and operational activities among the PI, research team members, collaborators, and external partners, including meetings, agendas, communications, documentation, and project updates
- Assisting with research administration by preparing budgets, annual reports, progress reports, grant submission materials, and other required documentation
- Preparing the initial IRB documents, assuring necessary approval, adhering and maintaining on-going IRB standards
- Performing duties in conjunction with evidence-based supported employment principles and the individual treatment plan, and coordinated through and with the clinical team
- Performing additional research-related duties as assigned to support program goals and objectives
Work Schedule: Monday to Friday; 08:00 a.m. to 04:30 p.m.
Recruitment & Relocation Incentives: Not authorized
Critical Skills Incentive (CSI): Not Approved