Research Coordinator - INSPIRE at Institute of Human Virology, Nigeria

Summary/Overview

• The Research Coordinator works with and under the direction of the Principal Investigator (PI), INSPIRE NIH R01 – 1R01AI147331-01.
• The Research Coordinator will support, facilitate and coordinate daily clinical trial activities.
• S/he will work with the PrincipaI Investigator of the study, research sponsor and institution and colleagues to support and provide guidance on aspects of the study e.g administration of the compliance, finance and personnel.
• The Research Coordinator will be responsible for the coordination and implementation of the program plan, coordinating core teams, arranging network meetings, coordinating training evaluations, monitoring of programs and ensuring that all program milestones are met.
• S/he will ensure that budget and reports timelines are met and a good working relationship established with Key Project Personnel.
• The Research Coordinator will report primarily to the Principal Investigator with associated responsibilities to the Department Head, Division Administrator or Program administrator.

Essential Functions

• Collaborate with the PI, department, and institutional administration to ensure that clinical research and related activities are performed in accordance with federal regulations and sponsoring agency policies and procedures.
• Collaborate with the PI to prepare Institutional Review Board /FCT Health Research Ethics Committee/National and any other regulatory submission documents as required by the protocol.
• Assist the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, execution of research plan. Maintain documentation of training. Provide appropriate training and tools for study team members.
• Ensure the efficient day-today operation of research activities and serve as the point of contact for internal study staff
• Monitor and maintain records of the progress of research activities, prepare periodic reports
• Collaborate with PI and institution to respond to any audit findings and implement approved recommendations.
• Collaborate with the PI and department to prepare a categorized budget and justification. Confirm accuracy and completeness of budgeted costs.
• Attend investigator meetings as required or requested by the PI.
• Prepare other study materials like informed consent documents case report forms (CRFs), enrollment logs, and drug/device accountability logs.
• Assist PI in submission of informed consent documents to Human Research Protection Office (HRPO) for review and approval.
• Establish and organize study files, including, regulatory binders, study specific source documentation and other materials.
• Screen subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
• Assist PI in communication of study requirements to all individuals involved in the study. Maintain study timelines and adequate inventory of study supplies.
• Plan and coordinate regular advisory board and steering committee meetings.
• In conjunction with the PI, execute targets within agreed time lines.

Qualification

• Must hold a M.Sc / MPH in Epidemiology, Biostatistics or Implementation Science.