leadership, professors, physicians, students, research participants, biostatisticians, etc.

Duties & Responsibilities:

• The Research Project Coordinator II is responsible to effectively operate and troubleshoot research specific equipment, software, and hardware. This position must be very technology savvy.
• The Research Project Coordinator II is responsible for knowing, following, and update research project standard operating procedures.
• The Research Project Coordinator II is responsible for ensuring research project activities, contracts, and agreements execute accordance with ATSU, state and, federal laws, policies, and guidelines.
• Evening and weekend work will be required infrequently.
• 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 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 documentation, preparing for audits and monitoring visits from regulatory bodies.
• Ensure all contractual and legally binding agreements execute per 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, 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.
• 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) web site.

Experience & Education:

• 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 posess strong initiative, use independent judgment, and be a team player.

leadership, professors, physicians, students, research participants, biostatisticians, etc.

Duties & Responsibilities:

• The Research Project Coordinator II is responsible to effectively operate and troubleshoot research specific equipment, software, and hardware. This position must be very technology savvy.
• The Research Project Coordinator II is responsible for knowing, following, and update research project standard operating procedures.
• The Research Project Coordinator II is responsible for ensuring research project activities, contracts, and agreements execute accordance with ATSU, state and, federal laws, policies, and guidelines.
• Evening and weekend work will be required infrequently.
• 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 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 documentation, preparing for audits and monitoring visits from regulatory bodies.
• Ensure all contractual and legally binding agreements execute per 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, 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.
• 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) web site.

Experience & Education:

• 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 posess strong initiative, use independent judgment, and be a team player.