Clinical Trials Administrator

Roles & ResponsibilitiesWe are looking for an Assistant / Manager with sufficient professional experience and stature to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore. The role will mainly assist our Clinical Trials Office to review and finalize contracts related to...

Roles & ResponsibilitiesResponsibilitiesProvide day-to-day departmental/project support activities, such as managing study supply inventory and orders, shipping, filing, faxing, etc.; Coordinate and provide minutes for department/project meetings or conference calls; Conduct quality review of documents; Maintain databases/spreadsheets and compile reports;...

About the RoleThis Clinical Trials Assistant position requires a motivated and detail-focused individual to support the smooth operation of our clinical trials. The successful candidate will have excellent organizational skills, strong communication abilities, and the capacity to work effectively in a team environment.Key DutiesSchedule appointments for...

Roles & ResponsibilitiesOverviewThe Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore and establish important capabilities for a future-ready healthcare system. The Business Entities under CRIS...

Roles & ResponsibilitiesInterested applicants are invited to apply directly at the NUS Career PortalYour application will be processed only if you apply via NUS Career PortalWe regret that only shortlisted candidates will be notified.Job SummaryWe are seeking a Master’s/PhD level Clinical Trials Biostatistician to support the design, analysis, and...

We are seeking an experienced Clinical Trials Coordinator to join our team at Kite. In this role, you will be responsible for managing patient cases from enrollment to delivery to the hospital, including reviewing each case upon receipt of referral and determining appropriate next steps based on defined process.You will work closely with healthcare providers...

Join Our Team: Kk Women's And Children's Hospital Pte. Ltd. is seeking a highly skilled Clinical Research Coordinator to join our research team.Responsibilities: Administer clinical trials in accordance with ICH-GCP and protocol requirements.Support the submission process for materials to CIRB and/or HSA on behalf of sponsors and PIs.Manage complex...

Roles & ResponsibilitiesAs a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.You will support and assist the Principal...

Roles & ResponsibilitiesAs a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.You will support and assist the Principal...

About the Role: We are seeking a highly skilled Clinical Research Coordinator to join our team at Kk Women's And Children's Hospital Pte. Ltd. As a key member of our research team, you will provide critical support for clinical trials and studies, ensuring compliance with ICH-GCP and protocol requirements.Main Responsibilities: Administer clinical trials in...

Job Summary The ideal candidate will provide research support services for clinical trials and studies, adhering to ICH-GCP and protocol requirements. This role involves independently administering clinical trials, assisting with submission processes, handling complex commercial or industry-initiated trials, and ensuring accountability of study equipment....

Roles & ResponsibilitiesResponsibilities:Provide research support service for clinical trials/research in accordance to ICH-GCP and protocol requirements Independently responsible for administration of clinical trials as assigned by Principal Investigator (PI) at his/her professional discretion Assist the sponsor or PI in the submission process for CIRB...

Roles & ResponsibilitiesJob Title: Operation AssociateSalary: Up to $2,800/monthWorking Hours: 8:00 AM - 5:00 PM (Monday - Friday)Job Description:Join a global leader in drug delivery technology and development solutions for pharmaceutical products. We are seeking a dedicated and meticulous Operation Associate to perform key operational processes in the...

Roles & ResponsibilitiesResponsibilities: Provide research support service for clinical trials/research in accordance to ICH-GCP and protocol requirements Independently responsible for administration of clinical trials as assigned by Principal Investigator (PI) at his/her professional discretion Assist the sponsor or PI in the submission process for CIRB...

Roles & ResponsibilitiesJob DescriptionYou will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile...

Roles & ResponsibilitiesJob SummaryAssist principal investigators and research teams in the conduct / implementation of all aspects of clinical research / clinical trials Venepuncture, handling and processing of blood samples / human specimens, recording ECG and monitoring vital signs Ensure all procedures are conducted in accordance with study protocols...

Roles & ResponsibilitiesJob Summary Assist principal investigators and research teams in the conduct / implementation of all aspects of clinical research / clinical trials Venepuncture, handling and processing of blood samples / human specimens, recording ECG and monitoring vital signs Ensure all procedures are conducted in accordance with study protocols...

Roles & ResponsibilitiesJob DescriptionYou will assist Principal investigators in conducting clinical trials & research projects according to Singapore Good Clinical Practice (GCP) guidelines. You will plan, organise & coordinate workflow of study projects from initiation to completion phase, perform screening and recruitment activities as well as compile...

Roles & ResponsibilitiesResponsibilities:Receptionist duties - Good standard of customer service - greeting and assisting patient enquiries - answering phone calls, emails and texts; registration and scheduling patients; handling billing and transactions; keeping patient records and paperwork organized. Assisting Chiropractors when required. Tidying up of...

Roles & ResponsibilitiesEnsuring study entry criteria and informed consent procedures are fulfilled Coordination and Scheduling of visits to various sites Organize and participate in site initiation visit. Work in collaboration with study team to ensure trial preparedness. Play a role in developing and implementing recruitment plan to ensure long-term...