Research Program Analyst, Safety & Compliance (Neurology) - #Staff

We are seeking a Research Program Analyst who will lead a specialized function in a research program that may include data management planning, research design, data driven program evaluation, optimizing funding opportunities and/or other technical duties that contribute to the quality and advancement of the research.Specific Duties & ResponsibilitiesIdentify research initiatives and inquiries to advance and assess the research priorities of the facultyLead research initiatives, e.g. data management activities, program evaluation, internal and external reportingContribute to the preparation and writing of reports to funders, manuscripts for publication, and presentations for internal and professional meetings.Provide and/or contribute to mentoring and training efforts.Consult with and advise faculty and leadership on systems, policies and practices key to research success.Other duties as assigned.In addition to the duties described aboveParticipate in scientific discussions with collaborators, study teams, and PICollaborate with study teams and PI to ensure operational feasibility of proposed protocol/study design (Risk Assessment)Develop or oversee the development of SOP, Data Safety Monitoring Plan (DSMP), Risk Management Plan (RMP) and inform the overall development of the study protocol, case report form (CRF) design, and safety surveillance tables, listings, and figuresMonitor activities, systems, and processes specific to safety-related events and protocol compliance through the clinical trial lifecycle, including but not limited to,Assist in identifying and evaluating trial risks associated with trial design and operations and the variables that impact the primary efficacy endpoint and critical safety parametersTrack to completion safety event reviews for multiple clinical trials in real time, assisting with collection of information for assessment adjudication by an independent medical monitorEnsure on time reporting of specific safety-related events to the Institutional Review Board (IRB), DSMB, Federal Drug Administration (FDA), and sponsors as determined by the protocolAssist in surveilling safety data for the identification of trends and communicate with study teams and study leaderCollaborate in study operational meetings to review safety and protocol compliance data, engage study teams in evaluating findings, and collectively determine and implement operational improvementsMinimum QualificationsMaster's Degree in a related field.Five years of related experience in research focus area.Additional education may substitute for required experience and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.Preferred QualificationsAuthorship on articles published in peer-reviewed journals.Experience writing manuscripts and grants.Classified Title: Research Program AnalystJob Posting Title (Working Title): Research Program Analyst, Safety & Compliance (Neurology)Role/Level/Range: ACRP/04/MEStarting Salary Range: $64,600 - $113,300 Annually ($89,000 targeted; Commensurate w/exp.)Employee group: Full TimeSchedule: M-F 8:30 am - 5:00 pmFLSA Status: ExemptLocation: RemoteDepartment name: SOM Neuro BIOSPersonnel area: School of MedicineEqual Opportunity EmployerAll qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.J-18808-Ljbffr