Research Assistant

Columbia University
United States, New York, New York
Nov 14, 2024
Job Type: Support Staff - Union Bargaining Unit: SSA Regular/Temporary: Regular End Date if Temporary: Hours Per Week: 35 Standard Work Schedule: Building: Salary Range: $59,845.49 - $59,845.49 The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. Position Summary The Research Assistant will provide technical and research-oriented support focusing on a PCORI-funded study comparing brief interventions (Safety Planning Intervention plus follow-up contact vs. ultra-brief Interpersonal Psychotherapy for Adolescents, crisis version) with youth aged 12-19 presenting to the emergency department for suicidal ideation and behavior. This full-time position involves assisting in all aspects of study coordination for a complex, multi-site longitudinal clinical trial. The candidate will assist the Principal Investigator, Laura Mufson, PhD, Co-Investigator, Christa Labouliere, Ph.D. and the Columbia PCORI team providing support with participant recruitment, data collection, follow-up assessments, and study logistics, among other tasks. This position offers valuable experience in assisting with a multi-site randomized clinical trial focused on preventing suicidal behavior in adolescents and young adults. Responsibilities 25% - Support study team in coordinating within- and across-site communication regarding subject screening, recruitment, scheduling, data collection, and outreach. 25% - Maintain documentation of all participant interactions/activities, regulatory binders/clinical trials research compliance documentation, and participant records. 20% - Assist in collection, entry, management, and integrity checks of study data in REDCap, including coordinating data collection and maintaining study records/databases. 10% - Schedule and conduct study procedures, including engaging in participant outreach and maintaining contact through the study period. 5% - Coordinate IRB submissions, renewals, and amendments. 10% - Assist in preparation of data for analysis; assist in writing reports and drafting of manuscripts and conference presentations 5% - Performs related duties & responsibilities as assigned/requested. Minimum Qualifications Bachelor's degree and at least one and one-half years of related experience or equivalent in education, training and experience. Knowledge of various related laboratory procedures and techniques required. Preferred Qualifications Master's degree in psychology or a related area. 1-2 years experience in research, preferably clinical trials research with children or adolescents. Comfortable interacting with youth and their families with mental health concerns (with training and supervision). Experience completing IRB applications, renewals, and amendments. Experience maintaining regulatory binders and clinical trials participant records. Experience completing project compliance and reporting requirements. Experience with data analysis and management. Bilingual in Spanish. Other Requirements Very organized and detail-oriented. Clear and frequent communication. Ability to multi-task and problem-solve in a fast-paced environment. Able to liaise and coordinate with participants, collaborators, and stakeholders. Organizing and coordinating schedules. Collecting/managing data across multiple participants and sites over time Able to effectively use Microsoft computer software (Word/Excel/Powerpoint), SPSS, and REDCap. Equal Opportunity Employer / Disability / Veteran Columbia University is committed to the hiring of qualified local residents.