









We are seeking two (2) motivated Clinical Research Interns to join our team. These internships aim to equip the candidates with essential skills for the successful execution of clinical study activities. Responsibilities: This role will support and collaborate with GCTO stakeholders at local level to ensure the smooth conduct of clinical studies. * Assist CRAs/ CTCs with daily study activities. * Support the collection, review, and monitoring of essential documentation for the study start-up, maintenance, and close-out phases. * Support with the preparation of regulatory documentation for studies in the validation phase. * Assist with document management within electronic Trial Master Files (eTMF) and electronic Investigator Site Files (eISF), including the preparation, distribution, and archiving of clinical documents. * Assist to management and maintenance of information in CTMS, CLMS and various other systems as appropriate and per timelines. * Support System SMEs in system clean-up activities. * Support the collection of information necessary for budget customization. * Provide assistance for various study tasks, as needed, in collaboration with other sponsor roles to achieve study milestones effectively.