ATSU – Research Project Coordinator II

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first_imgA.T. Still University of Health Sciences (ATSU) is seekingapplications for a Research Project Coordinator II on the Mesa,Arizona campus. The Research Project Coordinator II is responsiblefor the successful planning and implementation for multiple ATSUsclinical and academic Research Support projects. Research Supportprojects and associated phases must be planned, monitored, andcontrolled, whereby they are delivered on time and following therespective research protocols. The Research Project Coordinator IIis responsible for constant communications to all ATSU and externalstakeholders. This includes but not limited to, senior leadership,professors, physicians, students, research participants,biostatisticians, etc.Job Duties:The Research Project Coordinator II is responsible toeffectively operate and troubleshoot research specific equipment,software, and hardware. This position must be very technologysavvy.The Research Project Coordinator II is responsible for knowing,following, and update research project standard operatingprocedures.The Research Project Coordinator II is responsible for ensuringresearch project activities, contracts, and agreements executeaccordance with ATSU, state and, federal laws, policies, andguidelines.Evening and weekend work will be required infrequently.Lead, plan, implement, and execute research projects tosuccessfully meet research study objectives.Lead and assist with a variety of research program events.Effectively learn, operate, train, and troubleshoot researchlab equipment, software, and hardware.Organize and lead research project status meetings with timelyfollow up to ensure deadlines are achieved.Effective written and oral communications with research projectstakeholders.Provide consultation to principal investigator(s) and other keystakeholders (e.g., research team members, funders, regulatorybodies) on study-specific research processes Research study datacollection planning, including data management and data qualitymanagement.Processing collected data using project-specific procedures andtechnology.Recruit, screen, and enroll research participants.Ensure compliance with all regulatory activities and duties, atinstitutional, local, and/or national levels, including creatingand submitting IRB applications and maintaining IRB approvals,communicating adverse events, maintaining procedural documentation,preparing for audits and monitoring visits from regulatorybodies.Ensure all contractual and legally binding agreements executeper ATSU, state, and federal (FDA, NIH, OHRP) policies.Effectively manage fiscal and physical research resources,including preparation and submission of required statusreports.Effectively manage study finances including invoicing andresolving study subject compensation issues.Train, educate, mentor, and supervise research studypersonnel.Act as a liaison for research subjects, investigators, IRB,sponsors, funders, collaborators, and healthcare professionals,ensuring effective communication with all stakeholders.Coordinate academic research tests and testing protocol withthe curriculum department and course instructors.Evening and weekend work will be required infrequently.Writing semi-annual and annual reports to regulatory bodies andfunding agencies.Evaluating the feasibility of industry-sponsored pharmaceuticaland device clinical trials.Develop study/project advertisement materials.Update Research Support intra-net (ATSU internal) website.Skills/Requirements:Bachelor’s degree (Science or health-related field preferred)plus postgraduate studies required; MA or MS preferred.ACRP or SOCRA certification preferred.Strong Information Technology (IT) understanding.Relevant experiences in clinical/academic researchrequired.Experience in screening and consenting patients for researchparticipation.Experience in grant implementation and monitoring budgetarycosts.last_img

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