>Assigned as a Regional Clinical lead for trials conducted in Asia>Coordinates the Clinical team and support the Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible for the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are… Show more >Assigned as a Regional Clinical lead for trials conducted in Asia>Coordinates the Clinical team and support the Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible for the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are met>Responsible for training the team>Responsible for reviewing visit reports >Create clinical management plan, additional guidelines/ instructions for the CRAs>Mentors junior CRAs>Perform QCs on study files Show less

>Assigned as a Regional Clinical lead for trials conducted in Asia>Coordinates the Clinical team and support Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible for the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are met>Responsible… Show more >Assigned as a Regional Clinical lead for trials conducted in Asia>Coordinates the Clinical team and support Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible for the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are met>Responsible for training the team>Responsible for reviewing visit reports >Create clinical management plan, additional guidelines/ instructions for the CRAs>Mentors junior CRAs>Perform QCs on study files Show less

>Coordinates the Clinical team and support Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are met>Responsible for training the team>Responsible for reviewing visit reports… Show more >Coordinates the Clinical team and support Project Leader>Responsible for achieving the milestones of the project in accordance with contracted scope of work, budgeted hours and timelines>Responsible the maintenance of high quality deliverables, including preparation and attendance to audits and inspections>Ensure that timeline, quality and productivity of the projects are met>Responsible for training the team>Responsible for reviewing visit reports >Create clinical management plan, additional guidelines/ instructions for the CRAs>Mentors junior CRAs>Perform QCs on study files>Super user for PAREXEL Clinical Trial Management System (IMPACT) lead for Singapore and providing guidance and training to all Clinical Research staff in the office including Project Leads and Department Heads. Show less

>Works in accordance with ICH Guidelines and SOPs and was involved in the quality control check and maintenance of study files >Attend all study related meetings, internal calls and Client conference>Update project tools.>Present at Investigators and CRAs meetings>Involved in the feasibility, site selection, pre-study visits at site>Accountable for detecting, analyzing and solving technical, procedural and/or motivational problems that may occur to the site… Show more >Works in accordance with ICH Guidelines and SOPs and was involved in the quality control check and maintenance of study files >Attend all study related meetings, internal calls and Client conference>Update project tools.>Present at Investigators and CRAs meetings>Involved in the feasibility, site selection, pre-study visits at site>Accountable for detecting, analyzing and solving technical, procedural and/or motivational problems that may occur to the site staff of the investigation team Show less

>Monitoring of subjects during trial to ensure their compliance to the protocol>Process and storage of samples from subjects during intervals in accordance to the protocol for researchers’ analysis using HPLC.