ATSU - Research Project Coordinator II

About the role

The Research Project Coordinator II is responsible for the successful planning and implementation of 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.

Responsibilities

• Effectively operate and troubleshoot research specific equipment, software, and hardware.
• Know, follow, and update research project standard operating procedures.
• Ensure research project activities, contracts, and agreements execute according to ATSU, state, and federal laws, policies, and guidelines.
• Lead, plan, implement, and execute research projects to successfully meet research study objectives.
• Lead and assist with a variety of research program events.
• Organize and lead research project status meetings with timely follow up to ensure deadlines are achieved.
• Provide consultation to principal investigator(s) and other key stakeholders on study-specific research processes.
• Process 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 documentation, preparing for audits and monitoring visits from regulatory bodies.
• Manage fiscal and physical research resources, including preparation and submission of required status reports.
• Manage study finances including invoicing and resolving study subject compensation issues.
• Train, educate, mentor, and supervise research study personnel.
• Care for and maintain relationships with research subjects, investigators, IRB, sponsors, funders, collaborators, and healthcare professionals, ensuring effective communication with all stakeholders.
• Coordinate academic research tests and testing protocol with the curriculum department and course instructors.
• Write semi-annual and annual reports to regulatory bodies and funding agencies.
• Evaluate the feasibility of industry-sponsored pharmaceutical and device clinical trials.
• Develop study/project advertisement materials.
• Update Research Support intra-net (ATSU internal) web site.

Requirements

An associate's degree or higher preferred. Three to five years experience in leading and organizing multiple research studies and projects effectively. Effective and confident speaking, writing, and presentation skills. Relevant experiences in clinical/academic/health sciences research. Strong attention to detail. Must possess strong initiative, use independent judgment, and be a team player.

Qualifications

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Skills

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Benefits

ATSU offers a comprehensive benefits package including medical, dental, and vision coverages, among more. If eligible, employee-elected benefits would begin the first of the month following hire date. For more information, please visit: atsu.edu/employment/benefits.

Pay

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Schedule

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