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...

**Job Title**Manager, Clinical Research Networks (3 year contract) **About SCRI** The Singapore Clinical Research Institute (SCRI) is the national coordinating body (NCB) for clinical trials with a vision to establish Singapore as a regional thought leader in clinical research. This is accomplished through the deployment of innovative technologies...

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 & 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 & 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 & 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...

Roles & ResponsibilitiesYou will serve as part of the research team involved in clinical qualitative and/or quantitative research. Your job scopes include patient education, taking consent, performing interviews, evaluation and investigations; recording findings, maintaining equipment, optimising resources, scheduling appointments, preparing set-up 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...

**Address of office: 30 Loyang way, Unit 02/12-15, Singapore 508769 At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and...

National Neuroscience Institute of Singapore **Clinical Research Coordinator II**: - Job Category: Research - Posting Date: 5 Mar 2025 There will be opportunities to: - Perform study procedures, such as obtaining informed consent and recruitment of study participants, administer study questionnaires, coordinate follow-up visits, monitoring of adverse...

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...

Roles & Responsibilitiesup to 3800West CentralBe involved in subject recruitment, scheduling and data entry. Screen patients based on study eligibility, and communicate the study aims to potential subjects in layman terms. Obtain consent taking, administer study questionnaires and follow-up on study participants. Work closely with research team,...

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...

**Overview** 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. The Business Entities under CRIS include: - Singapore Clinical...

Roles & ResponsibilitiesThe incumbent will work as part of an established and nationally funded multi-disciplinary research group that focuses on hepatocellular carcinoma (HCC). You will support the research team in coordinating the investigator-initiated trial activities. The successful candidate will thrive in a dynamic and collaborative research...

**Clinical Research Intern** MiRXES is a Singapore-headquartered molecular diagnostic company with R&D, manufacturing, and clinical lab operations in Singapore, USA, Japan, and China. We specialize in microRNA technologies and the development, manufacturing, and provision of diagnostic test kits and clinical services. Our mission is to enable early disease...

**DESCRIPTION** The Clinical Research Associate (CRA) - Site Manager will coordinate clinical studies and be responsible for all major stages of study development, execution, monitoring, and close-out. **RESPONSIBILITIES**: - Drafts materials including informed consents, case report forms (CRFs), CRF completion guidelines, and technical instructions. -...

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...