The Public Health Institute (PHI) is an independent, nonprofit organization dedicated to promoting health, well-being, and quality of life for people throughout California, across the nation and around the world. As one of the largest and most comprehensive public health organizations in the nation, we are at the forefront of research and innovations to improve the efficacy of public health statewide, nationally, and internationally.
PHI was distinguished as one of the top 50 "Best Non-Profit Organizations to Work For" by the Non-Profit Times in a national search.
Position Summary The Children's Oncology Group (COG), a National Cancer Institute supported clinical trials group, is the world's largest organization devoted exclusively to childhood and adolescent cancer research. The COG unites more than 10,000 experts in childhood cancer at more than 200 leading children's hospitals, universities, and cancer centers across North America, Australia, and New Zealand in the fight against childhood cancer. Our goal is to cure all children and adolescents with cancer, reduce the short and long-term complications of cancer treatments, and determine the causes and find ways to prevent childhood cancer.
The Research Coordinator (RC) serves as the data management specialist on the study team (Protocol Coordinator, Research Coordinator, Study Builder and Statistician) for all assigned COG trials. This position is responsible for coordinating all aspects of data acquisition and management for assigned COG studies under the direction of the Study Chair, Study Statistician, COG/Scientific Committee leadership, and other staff responsible for implementing and conducting COG studies. This involves developing, testing, and implementing Case Report Forms (CRFs), data validations, and data management plans (DMP) for assigned COG studies. It also involves monitoring the quality and timeliness of submitted study research data, overseeing subject enrollments/randomizations, conducting data cleaning activities, and coordinating central reviews within COG Electronic Data Capture systems (EDC) for all assigned studies. The Research Coordinator is also required to amend CRFs per study needs, implementing the corresponding changes in the EDC system and DMP.
This is a remote regular full-time position.
Full salary range for this position: $62,968 to $90,167 per year. The typical hiring range for this position is from $62,968 (minimum) to $76,568 (midpoint), based on 100% FTE. The starting salary is determined based on the candidate's knowledge, skills, experience, as well as budget availability.
Minimum Qualifications Two (2) years of human clinical trial research experience. A combination of relevant master's degree and experience may be used to meet the two-year human clinical trial research experience requirement. Bachelor's degree in a related field, or substitute with four additional years of relevant experience. Other Qualifications Experience as a Clinical Data Manager or Clinical Research Coordinator is preferred. Experience in a comprehensive cancer center, cooperative group or pharmaceutical/biotechnology industry is highly desirable. Strong organizational skills with the ability to handle a variety of tasks and work independently. High level of PC literacy is needed, including broad knowledge of Microsoft Office software (MS Word, Excel, and PowerPoint). Excellent written and oral communication skills. Critical thinking and reasoning.
#J-18808-Ljbffr
