ATSU
– Research Project CoordinatorJob Category: Research/GrantsRequisition Number: ATSUR001983Full TimeKirksville, MO 63501, USAKirksville, MO 63501, USA Job Details Description A.T.
Still University (ATSU) is seeking a Research Project Coordinator II on the Kirksville, Missouri, campus.
The position is responsible for the successful planning and implementation of multiple ATSU clinical and academic projects.
Such must be planned, monitored, and controlled, whereby they are delivered on time and follow the respective research protocols.
The Research Project Coordinator II is responsible for constant communications to all ATSU and external stakeholders.
This includes but is not limited to senior leadership, professors, physicians, students, research participants, statisticians, etc.
The position is also responsible for effectively operating and troubleshooting research-specific equipment, software, and hardware.
The individual must be very technology savvy.
The Research Project Coordinator II is responsible to know, follow, and update research project standard operating procedures.
The position is responsible to ensure research project activities, contracts, and agreements are executed in accordance with ATSU, state, and federal laws, policies, and guidelines.
Evening and weekend work will be required infrequently.
Major Job Duties Lead, plan, implement and execute research projects to successfully meet research study objectives Lead and assist with a variety of research program events Effectively learn, operate, train, and troubleshoot research lab equipment, software, and hardware Organize and lead research project status meetings with timely follow up to ensure deadlines are achieved Effective written and oral communications with research project stakeholders Provide consultation to the principal investigator(s) and other key stakeholders (e.g., research team members, funders, regulatory bodies) on study-specific research processes Research study data collection planning, including data management and data quality management Processing collected data using project-specific procedures and technology Recruit, screen, and enroll research participants Ensure compliance with all regulatory activities and duties, at institutional, local, and/or national levels, including creating and submitting IRB applications and maintaining IRB approvals, communicating adverse events, maintaining proceduraldocumentations, preparing for audits, and monitoring visits from regulatory bodies Ensure all contractual and legally binding agreements are executed in accordance with ATSU, state, and federal (FDA, NIH,OHRP) policies Effectively manage fiscal and physical research resources, including preparation and submission of required status reports Effectively manage study finances including invoicing and resolving study subject compensation issues Train, educate, mentor, and supervise research study personnel Act as a liaison for research subjects, investigators, IRB, sponsor, funders, collaborators, and healthcare professionals ensuring effective communication with all stakeholders Coordinate academic research tests and testing protocol with curriculum department and course instructors Evening and weekend work will be required infrequently Writing semi-annual and annual reports to regulatory bodies and funding agencies Evaluating the feasibility of industry-sponsored pharmaceutical and device clinical trials Develop study/project advertisement materials Update Research Support intra-net (ATSU internal) website Skills/Requirements Four year college degree, science or health-related field preferred M.A.
or M.S.
degree preferred Certification by ACRP or SOCRA preferred Certification in project management preferred Very strong IT skills preferred Knowledge and experience in clinical and academic research Certificate from an accredited organization, such as the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SOCRA) would be helpful Knowledge of legal and regulatory issues in clinical research as well as a clinical research methodology Strong Information Technology (IT) understanding Knowledge and experience with project management best practices Experience in grant implementation and monitoring budgetary costs Experience with healthcare, clinical research, and study monitoring Experience in screening and consenting patients for research participation Positive, outgoing attitude Ability to excel in a complex, detail-oriented environment Effective and confident speaking and presentation skills Relevant experiences in clinical/academic research Use of independent judgment Project management best practices Discretion communications Time management skills to implement and manage a research study Be very computer literate Proactive Be familiar with budget management Outgoing and personable Challenges the status quo Industrious Highly professional Organize and lead effective team meetings Ability to multitask as a team player but also use independent judgment to make important decisions and workindependently Tactful Works well under pressure Ability to work well with persons of diverse educational, socioeconomic, and ethnic backgrounds Flexible and open to change Ability to recognize and overcome potential obstacles Driven Polite Qualifications Skills Required Flexibility Intermediate Critical Thinking Intermediate Multitasking Intermediate Confidence Intermediate Verbal Communication Intermediate Written Communication Intermediate Problem Solving Ability Intermediate Initiative Intermediate Research Intermediate Presentation Intermediate Speaking Intermediate Positive Attitude Intermediate Preferred Respectful Intermediate Self-Motivation Intermediate Behaviors Required Detail Oriented: Capable of carrying out a given task with all details necessary to get the task done well : Motivations: Education Required Bachelors or better in Health Sciences or related field.Preferred Masters or better.Experience Required 3-5 years: Relevant experiences in clinical/academic research 3-5 years: Effective and confident speaking and presentation skills 3-5 years: Strong IT background 3-5 years: Experience in coordinating, leading, and organizing multiple projects effectively Licenses Certifications To apply, visit https://recruiting2.ultipro.com/ATS1000ATSU/JobBoard/3cecd56d-0475-4bd9-8534-c2eb468057dd/OpportunityDetail?opportunityId6c69c090-d8c2-4988-b827-eaba8da6d406Copyright ©2022 Jobelephant.com Inc.
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