Clinical Trial Assistant

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...

**Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

**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...

The position is responsible for providing clerical, administrative, and technical administrative support to one or more business units or clients within Clinical Operations. - Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions - Assists Clinical...

Join to apply for the Clinical Lead role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We advance clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic...

Join to apply for the Clinical Lead role at Emerald Clinical At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We advance clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic...

**Job Overview: **Key Responsibilities**: - Serve as the unblinded point of contact for logistics vendors and unblinded CRAs. - Generate and review shipment documents, including batch records, Certificate of Conformance (CoRC), temperature logger data, etc. - Manage investigational product (IP) inventory and ensure proper storage and distribution. - File...

**Responsibilities**: - Assist Clinical Team with accurately maintaining clinical trials documents (E.g TMF) for various projects including preparation, handling, distribution, filing of clinical documentation and periodic review and QC check of study files for accuracy, completeness and audit readiness. - Assist Clinical Team in liaison with external...

Prepare and submit clinical trial documents, amendments and approvals to the relevant parties. Recruit, schedule and screen participants for clinical trial projects. Data collection and management. Coordinate with sponsors, investigators, and internal teams to provide timely project status. Perform skin related measurements (hydration, elasticity..etc.)....

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...