You will be assigned to various parts of center in Singapore
Job Overview
i. Explain patient information leaflet and obtain informed consent from patients
ii. Manage randomization and informing team on the assigned arm
iii. Train patients on the completion of e-questionnaire (English only)
iv. Coordinate with team, follow-up and remind patients on scheduled follow-up visit back to (baseline, week 3, week 8)
v. Support patients in completion of e-questionnaire (baseline, week 3, week 8)
vi. Follow-up and remind patients on completion of e-questionnaire (month 3, month 6)
vii. Maintain site files including protocol signature, ICF, patient information list, protocol deviation, and quality log
The Clinical Trial Coordinator will provide project management, support and coordination of programmatic activities and contribute to patient engagement activities and clinical research support in healthcare sectorOther Essential Functions
Requirements
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com