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 Project Coordinator II will manage day-to-day research and related administrative activities for two large-scale intervention trials funded by the National Institute of Mental Health (NIMH). Both are randomized control trials evaluating the effectiveness and implementation of mental health interventions for adolescents in Mozambique, in collaboration with the Mozambican Ministry of Health and ICAP Columbia. The Project Coordinator II will be based in the Department of Sociomedical Sciences (SMS) at the Columbia Mailman School of Public Health (MSPH), where they will serve the lead role for assisting both the MSPH research team and coordinating with the Mozambican Project Coordinator and field staff. In collaboration with study investigators, the Project Coordinator II will provide administrative oversight and high-level data management of the trials. Travel to Mozambique will occur twice per year, for
approximately 15 days of local field work each visit.
Responsibilities
Coordinate CUIMC-based clinical trial oversight in collaboration with study investigators and
field staff in Mozambique. This includes lead responsibility for data management, data quality
control, developing programs to monitor study progress that inform and enhance recruitment
and retention, problem-solving study implementation with field staff, and research team
communications. (40%)
Initiate high-level administrative tasks including scheduling, coordinating, and developing
agendas for all team meetings, assist in planning and monitoring budgets, develop drafts for all
NIH grant reporting (RPPR and RMR) and oversight of student workers. (20%)
Update research tools and study protocol and serve as the primary liaison with the CU
Institutional Review Board (IRB) while collaborating with Mozambican staff and their human
research ethics committee (CNBS). (10%)
Assist with literature reviews, background research, and writing of grants and manuscripts.
(10%)
Prepare full dataset in collaboration with biostatisticians for primary outcome analyses. Coauthor
manuscripts and develop materials for dissemination of findings to community partners.
(10%)
Support all clinical trial requirements, including monitoring and reporting of adverse events, Data
and Safety Monitoring Board (DSMB) reporting and clinicaltrials.gov. updates. (5%)
Perform general administrative functions, and related duties and responsibilities as assigned / requested. (5%)
Minimum Qualifications
Preferred Qualifications
Other Requirements
Equal Opportunity Employer / Disability / Veteran
Columbia University is committed to the hiring of qualified local residents.
Project Coordinator • New York, NY, United States