Job Description

The Research Project Coordinator II is responsible for the successful planning and implementation for multiple ATSUs clinical and academic Research Support projects. Research Support projects and associated phases must be planned, monitored, and controlled, whereby they are delivered on time and following the respective research protocols. The Research Project Coordinator II is responsible for constant communications to all ATSU and external stakeholders. This includes but not limited to, senior leadership, professors, physicians, students, research participants, biostatisticians, etc.

  • The Research Project Coordinator II is responsible to effectively operate and trouble shoot research specific equipment, software, and hardware. This position must be very technology savvy.
  • The Research Project Coordinator II is responsible to know, follow, and update research project standard operating procedures
  • The Research Project Coordinator II 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

Responsibilities:

  • 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 trouble shoot 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 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 procedural documentations, 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

Skills / Requirements

Three to five year experience and a four year college degree in science or health-related field preferred.