Clinical Research Coordinator

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 include: ...

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 include: ...

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...

About UsThe Consortium for Clinical Research and Innovation, Singapore (CRIS) is a leading organization that brings together six national R&D, clinical translation, and service programmes to advance clinical research and innovation in Singapore. Our mission is to establish important capabilities for a future-ready healthcare system.

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 & Responsibilities Liaison person with Principle Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc. Plan, organise and coordinate the workflow of the research study Adhere to protocol procedure Screen research participants for eligibility according to research...

Roles & ResponsibilitiesLiaison person with Principle Investigator (PI), site-PI and various departments for clinical research procedures e.g. Specialist Clinics, Laboratory, wards, etc. Plan, organise and coordinate the workflow of the research study Adhere to protocol procedure Screen research participants for eligibility according to research protocol ...

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...

Roles & ResponsibilitiesThe KKH Paediatric Allergy Service is looking for highly motivated and enthusiastic candidates with a keen interest in clinical research in allergic disease to join our team as a Clinical Research Coordinator (CRC). The CRC will be responsible to, and collaborate with, the Principal Investigator and study team members to conduct...

Company Overview: The Consortium for Clinical Research and Innovation, Singapore (CRIS) is a leading organization in advancing clinical research and innovation for Singapore. Our mission is to establish important capabilities for a future-ready healthcare system by ensuring that our clinical research platforms and programmes are at the cutting edge of...

Job OverviewClinical Trials Assistants play a pivotal role in ensuring the smooth operation of clinical trials. As a key member of our team, you will be responsible for assisting Clinical Research Associates and the Regulatory and Start-Up team with maintaining accurate and up-to-date clinical documents and systems. This includes tracking site compliance and...

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...

Job Description:As a Clinical Research Coordinator at Kk Women's And Children's Hospital Pte. Ltd., you will be responsible for providing research support services for clinical trials and studies in accordance with ICH-GCP and protocol requirements.Key Responsibilities:Administer clinical trials independently as assigned by the Principal Investigator (PI) at...

Roles & ResponsibilitiesAbout Us:Are you passionate about contributing to groundbreaking research projects that advance medical knowledge and improve patient care? Join our team as a Clinical Research Coordinator/Assistant and play a pivotal role in the development and execution of innovative research initiatives. We offer opportunities for individuals with...

About Us:The 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.Cris makes a positive difference to Singapore patients and researchers...

Job DescriptionThe Consortium for Clinical Research and Innovation Singapore is seeking a skilled Procurement and Logistics Professional to join our team. As a Senior/Executive, GMP Procurement, you will play a critical role in managing the sourcing activities, including publishing purchasing documents via our online procurement portal.Key...

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....

About the JobWe are seeking a highly skilled GMP Procurement and Operations Lead to join our team. The successful candidate will be responsible for leading the procurement and logistics operations, including material qualification, inventory management, and coordination with suppliers.Key Responsibilities:Lead the procurement and logistics operations,...

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...