Clinical Research Coordinator B
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Job Description Summary
The Department of Family Medicine and Community Health is seeking a Research Coordinator B to support and implement daily operations for diverse quantitative and qualitative research projects focused on improving the impact, quality, and implementation of cancer screening and care.
The Research Coordinator B will support and implement daily operations for diverse quantitative and qualitative research projects focused on improving the impact, quality, and implementation of cancer screening and care. In coordination with project principal investigators, project managers, and analysts, this position will help to manage a range of existing research project including a pilot trial to evaluate digital health interventions for patients with lung cancer, a multisite project to develop quality metrics for lung cancer screening, and a mixed methods project to develop implementation strategies to decrease delays in cervical cancer care in Sub-Saharan Africa. In addition to coordinating clinical trials, this individual will also support primary data collection by conducting interviews and surveys, and supporting mixed methods analysis. The person will 1) develop project documentation, including portions of project plans, study protocols, standard operating procedures, and IRB and other regulatory documents; 2) execute research project activities by initiating study procedures; conducting and overseeing recruitment, screening, enrollment, and follow-up procedures for study participants; and coordinating and conducting primary data collection and preparation; 3) draft reports, memos, abstracts, manuscripts, presentations, and proposals; and 4) coordinate meetings and track project tasks and deliverables; and implement other research activities as assigned.
Bachelor’s degree and 2-3 years of research experience in a clinical or academic setting or equivalent combination of education and related experience. Excellent written and verbal communication skills; strong organizational skills and attention to detail; demonstrated ability to problem solve and identify and utilize available resources; demonstrated ability to manage multiple priorities concurrently and coordinate project inputs and stakeholders; strong interpersonal skills, judgment, and diplomacy to work effectively with diverse internal and external stakeholders; proficiency with standard office software (Microsoft Word, Excel, PowerPoint, Outlook); and experience managing clinical trial or study protocols. Preferred qualifications: Master’s degree; experience conducting and analyzing qualitative data; knowledge of software for, electronic data capture (e.g., REDCap) and qualitative data analysis (e.g., NVivo, Atlas.ti).
This position is contingent upon funding.
Office, Library, Computer Room; Requires extensive safety
Typically sitting at a desk or table; Occasional lifting 25 lb. or less
Job Location - City, State
Department / School
Perelman School of Medicine
$42,953.00 - $77,315.00
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