Posted in Other about 2 hours ago.
Location: Portland, Oregon
The senior research associate (research program manager) is a highly organized and motivated clinical research professional who directs research operations and administrative efforts of the Busui research team. The position partners with Dr. Busui to establish the program’s focus on diabetes related research across the OHSU community and external partners. The senior research associate is responsible for establishing and formalizing relationships with regional and national collaborators. The position supervises work on multiple ongoing studies related to Diabetes and Diabetes Complications, as well as assisting with management of research grants and contracts in collaboration with administration from the Department of Medicine. The position will assist with managing the research group of study coordinators, volunteers, and student workers, including interviewing candidates, onboarding and training new staff, leading group meetings, and coordinating research efforts at other project sites. The senior research associate will be responsible for regulatory supervision and ensuring high quality data collection. The senior research associate will perform data analysis using qualitative and quantitative methods. The senior research associate will assist with submitting grant applications to federal, industry, and foundation sponsors, with responsibility for budget development and negotiation, collaborating on proposal development, and specific application requirements. The senior research associate will manage awarded funding, ensuring compliance with federal and sponsor-specific policies. This position will also support the growing research efforts as the department level from a collaboration, training and best practices sharing standpoint.
Strong interpersonal and critical thinking skills for independent problem solving, and an ethical approach to science and human subjects research, are needed to achieve scientific and administrative objectives.
Strong organizational skills and attention to detail.
Demonstrated ability to take initiative and complete projects independently or lead a team.
Excellent communication, both written and verbal with fluency in English. Strong computer skills and advanced MS Office skills.
Ability to navigate research site visits with industry sponsors, in-depth knowledge of budget development and clinical trial review.
Knowledge of institutional review board (IRB) processes for submitting, modifying, terminating and continuing review of human protocols.
Understanding of best practices for clinical research, including research ethics.
Project management skills, including use of management/organizational technology.
Working knowledge of FDA IDE/IND submission process, ONCORE, and experience with REDCap.
Familiarity with electronic medical records (preferably EPIC), chart review and medical terminology.
HR-related competencies including screening, interviewing, and onboarding research staff.
PI250354516
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