Clinical Research Coordinator

Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Assistant Manager, Clinical Research Outreach & Engagement (National Coordinating Office, SCRI)Overview The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance...

**Brief Position Description**: The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key...

Overview Clinical Research Coordinator responsibilities and related activities at the hospital/healthcare research program. Responsibilities Liaison with Principal 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...

Major Duties and Responsibilities Liaison person with Principal 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 & ResponsibilitiesMAJOR DUTIES AND RESPONSIBILITIES(A) SPECIFIC (90%) Liaison person with Principal 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...

Roles & ResponsibilitiesYou will assist the principal investigators in development and implementation of clinical research and clinical trial protocol including:Preparation of documents for and facilitation of regulatory (e.g. Institution Review Board, Health Sciences Authority) approvals Design and develop informed consent form, data collection forms, logs...

Our client in the healthcare industry is looking to hire Clinical Research Coordinators (CRC) to assist in a Human Biomedical Research study. As a CRC, you will be primarily responsible for subject recruitment and other research deliverables for the studies, and work closely with the research team and Principal Investigator. Responsibilities Be involved in...

Overview You 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 relevant patients' data and...

Overview You 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 relevant patients' data and...

As 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 Investigator in the...