Study Coordinator – CRITICal Project job at Infectious Diseases Research Collaboration (IDRC) | Apply Now

• Sensitization of districts, schools, and local stakeholders

• Oversee protocol implementation and ensure compliance with GCP and IRB guidelines

• Facilitate schoolchildren recruitment and informed consent

• Maintain trial documentation, including CRFs, consent forms, and regulatory binders

• Liaise with investigators, data managers, and ethics committees

• Provide day-to-day leadership and coordination of school Projects and school surveys

• Planning and budgeting for field activities

• Participation in the development of protocols, SOPs, and data collection tools

• Conducting data quality assessments, mentorship, and CMEs at schools and for the study team

• Presentation of updates and reports to the MoH technical working groups

• Ensuring proper administration of informed consent, and proper collection and management of data and samples from study sites.

• Prepare and distribute study updates and reports

• Oversee study drug quantification, transportation, storage, and administration

• Lead study team meetings

• Participate in data analysis, manuscript preparation, and dissemination of study findings in collaboration with the data management team and the investigators.

Key Result Areas/Outputs

• Leadership, supervision of staff, and team management

• Implementation of study activities, including surveys, data quality assessments, mentorship, CMEs, and other fieldwork

• Study drug management

• Data and sample management, including collection and analysis

• Report and manuscript writing

• Storage and maintenance of study documents, including informed consent forms and other regulatory files.