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About the Organisation
Study Coordinator – CRITICal Project job at Infectious Diseases Research Collaboration (IDRC) | Apply Now
Kampala, Uganda
The Infectious Diseases Research Collaboration (IDRC) is a non-profit research organization based in Uganda, dedicated to conducting high-quality research on infectious diseases such as malaria, HIV, and tuberculosis, aiming to improve public health outcomes through collaboration and partnerships. Established in 2007, IDRC has earned recognition for its significant contributions to infectious disease research, leading to over 300 publications that have influenced disease management practices in Uganda.
The organization fosters a work culture anchored in its I-TRAIN core values—Integrity, Teamwork, Respect, Accountability, and Innovation—promoting a supportive environment that emphasizes professional growth and excellence. IDRC offers diverse job opportunities across research, administration, and field operations, with work arrangements designed to accommodate both field-based and office-based roles. Since its inception, IDRC has expanded its reach across Uganda, collaborating with various national and international partners to enhance research capacity and public health interventions.
Its innovative business model integrates research with practical health solutions, ensuring that findings translate into tangible health improvements. Guided by core values such as integrity, excellence, and accountability, IDRC also engages in corporate social responsibility initiatives focused on community health education and sustainable development. For more information, visit their website at www.idrc-uganda.org.
Are you looking for Medical jobs in Uganda 2025 today? then you might be interested in Study Coordinator – CRITICal Project job at Infectious Diseases Research Collaboration (IDRC)
Full Time
Deadline:
30 Sept 2025
Job Title
Study Coordinator – CRITICal Project job at Infectious Diseases Research Collaboration (IDRC)
Infectious Diseases Research Collaboration (IDRC)
Job Description
Job Title: Study Coordinator – CRITICal Project
Organisation: Infectious Diseases Research Collaboration (IDRC)
Duty Station: Kampala, Uganda
Job Summary:
The Project Coordinator will play a key role in the CRITICal project, leading comprehensive Project activities
Duties, Roles and Responsibilities
Qualifications, Education and Competencies
See all details of the qualifications, competencies and education for this role under the "How to Apply" section below.
All suitably qualified and interested candidates should apply online at the APPLY Button below.
Deadline: 30th September 2025
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How to Apply
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.
Medical graduate (MBChB/MD or related field) with a Master’s in Public Health /Epidemiology/Biostatistics or related field.
Registration with the UMDPC & valid Annual Practicing License
At least 2 years’ experience in clinical research
Excellent interpersonal skills/Experience working with and leading teams
Excellent attention to detail
Must have good computer skills.
Strong skills in developing work plans, setting timelines, and tracking project progress
Exceptional organizational abilities to manage multiple projects and stakeholders efficiently
Proficiency in database management systems
Excellent communication skills for report writing, presentations, and engaging with partners, donors, and Ministry of Health officials
Must have valid GCP and HSP certificates

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