Clinical Trial Co-ordinator

Responsibilities:Prepare, draft, submit, and track clinical trial documents for submissions, amendments, and approvals with the relevant parties.Ensure all IEC correspondence, approvals, study documentation, and trial records are accurately maintained, filed, and properly archived.Coordinate with sponsors, investigators, and internal teams to provide timely...

Roles & Responsibilities Clinical Trial Co-ordinator Responsibilities: Prepare, draft, submit, and track clinical trial documents for submissions, amendments, and approvals with the relevant parties. Ensure all IEC correspondence, approvals, study documentation, and trial records are accurately maintained, filed, and properly archived. Coordinate with...

Overview Clinical Project Manager role at CTI Clinical Trial and Consulting Services. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the...

**Key Accountabilities**: Trial Preparation - Accountable for the trial activities for responsible R/OPU, including but not limited to; - Creation, management and review of the R/OPU trial budget to verify appropriate level of financial oversight and planning accuracy. Timely budget updates based on trial changes. - Appropriate trial-specific training of...

This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA. In this role, you will be involved in the process of supporting clinical trials for various therapies at the country level, and be the liaison between the site and Contract Research Organization (CRO) / Pharmaceutical...

National Heart Centre of Singapore Pte Ltd **Clinical Data Co-ordinator**: - Job Category: Administration - Posting Date: 5 Feb 2025 **Requirements**: - Good interpersonal and problem-solving skills - Resourceful, meticulous, willingness to learn and remains updated with new terminologies and domain knowledge

Key Accountabilities:Trial PreparationAccountable for the trial activities for responsible R/OPU, including but not limited to;Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities.Creation, management and review of the R/OPU...

Responsibilities 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 and regulations...

**Overview** The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together five 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...

-Family Group: Allied Health **Job 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...