Clinical Research Coordinator

Position Title: Clinical Research CoordinatorProject Title: A Protocol Comparing Temporary Transvenous Diaphragm Pacing to Standard of Care for Weaning from Mechanical Ventilation in ICU Patients (RESCUE 3)Employment Status: Part-Time (20 Hrs/Week)Position SummaryThe Clinical Research Coordinator will be working on multiple studies on behalf of the Principal Investigators. Responsibilities include, but are not limited to, the following: Coordination of research activities in existing and future research studies, including regulatory aspects; Recruiting, screening and enrolling study participants; Conducting study visits and collecting data; Participating in protocol training as required; and, Assisting with administrative research activities and tasks as needed.Job FunctionsJob Function 1 (40%): Overall coordination of research administrative activities associated with the study, including data management.Job Function 2 (40%): Interface with research participants and perform related tasks, such as identifying potential participants, conducting patient interviews/ questionnaires, collecting and processing samples (stool, blood, saliva), and collaborate with other coordinators to establish enrollment goals, etc.Job Function 3 (20%): Managing or assisting with regulatory submissions and the development/submission of protocols, including content revisions, protocol amendments, and continuing review applications to Emory IRB and the VA R&D Committee. Liaise between the regulatory committees, Atlanta VA site and study sponsor to communicate study progress and challenges.Other Functions: May perform administrative support/ tasks to ensure project and team success on an as needed basis. Minimum RequirementsEducation: Bachelor's degree is required. Candidates with degrees in a scientific, health-related, or business administration programs are preferred.Experience: 2+ years in research. Experience with clinical trials coordination and/or research administration is preferred. Regulatory experience is beneficial for the successful incumbent.Specific Skills: Must have strong organizational skills, detail-oriented, excellent oral and written communication skills. Proficiency in MS Office products (Word, Excel) and electronic health systems / databases.Special Knowledge: Certified Research Associate (CRA) or Clinical Research Coordinator (CRC) preferred.Relocation and Visa sponsorship are not available for this position. We are an equal opportunity employer with a commitment to diversity. All individuals, regardless of personal characteristics, are encouraged to apply.FAVER is an Equal Employment Opportunity/ Affirmative Action Employer. FAVER provides equal employment opportunities to all qualified applicants without regard to race, sex, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, or genetic information.