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Job Description: Project Coordinator:The World Health Research (WHR) Project Coordinator will play a pivotal role in managing and coordinating international randomized clinical trials. This position involves executing operational aspects of clinical trials, supporting the study team (project manager, research assistant, administrative assistant, etc.) in working with the study sites, trial sponsors, and external vendors, and maintaining effective communication between all stakeholders. Primary responsibilities of the role entail supporting clinical trials for WHR clients.The ideal candidate has extensive knowledge of clinical research principles, national and international regulatory guidelines, and industry best practices. The position requires the ability to work independently as well as collaboratively with cross-functional teams to ensure timely and accurate completion of tasks.Key Responsibilities:Project Management:Coordinate and manage assigned aspects of clinical research projects from initiation to completion, ensuring adherence to timelines and budgets.Material Development:Assist in the development of key materials, including study plans, informed consent forms, and other essential documents.Regulatory Compliance:Ensure all research activities comply with international regulations, Good Clinical Practice (GCP) guidelines, and institutional policies.Data Management:Work with trial sites to maintain accurate and up-to-date records of study data, including electronic data capture (EDC) systems. Review high level study reports to confirm accuracy in data reporting.Communication:Serve as the primary liaison between investigators, sponsors, regulatory agencies, and study participants.Monitoring: Oversee selection, training, recruitment, and follow-up of study participants across multiple centres and countries. Organize monitoring visits according to the established plan.Reporting:Track study progress, manage deviations, and report adverse events. Prepare regular progress reports for stakeholders.Mentoring:Supervise members of the study team, implement training plans, and oversee performance.Quality Assurance:Implement quality control measures to ensure the integrity and reliability of study data. Function as a subject matter expert for Standard Operating Procedures.Qualifications and Experience:Bachelors degree in health sciences or related area of study.Recent (3+ years) experience coordinating multi-centre research studies.Demonstrated experience managing large clinical research data sets.Demonstrated knowledge of ICH-GCP guidelines and international research requirements.Broad knowledge of research methodology, clinical trials, and drug development process.Demonstrated interpersonal, communication, and teamwork skills.Proficient in Microsoft Office Suite, electronic data capture (systems), and document management platforms.World Health Research: The members of World Health Research improve health through important research, education, and advocacy. A beacon of scientific rigour, the company is dedicated to supporting and championing transformative discoveries that reshape the medical landscape.Please send Resume and Cover Letter to