Clinical Trials Assistant

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies. **What you will be...

**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...

This Intern position reports to the Clinical Operations Manager and interfaces with the Site Management and Regulatory & Site Activation Team. The trainee will be involved in the process of managing clinical trials for novel therapies at the country level. **Assignment Scope & Learning Opportunities**: (Under the guidance) - Support of Clinical Trial...

**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,...

**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,...

Support trial during study start-up • Set-up Trial country relevant documents Create local signature page Set-up SharePoint, public drives, Microsoft Teams, etc. Enter feasibility tracking information to Client Clinical Trial Management System (CTMS) File Site qualification follow-up letter submission in Trial Master File (TMF) staging area ...

NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD is seeking a highly skilled Clinical Trials Specialist to join our team. As a specialist in clinical trial contract negotiations, you will play a crucial role in reviewing and finalizing contracts related to clinical trials for the Division of Clinical Trials & Epidemiological Sciences (CTE). The main duties...

Medpace Reference Laboratories (MRL) is a leading central laboratory with a strong presence in Singapore. We are seeking a skilled Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a critical role in supporting project management activities and contributing to the success of our organization.Main...

National Cancer Centre of Singapore Pte Ltd **Assistant / Manager (Clinical Trials Contract)**: - Job Category: Research - Posting Date: 21 Jan 2025 We are looking for an Assistant Manager OR Manager with sufficient professional experience and skills to fulfill a specialist role that can contribute to the development of the clinical trial program within...

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...

Job Description:The Clinical Research Coordinator is responsible for supporting clinical trial operations by coordinating participant recruitment, data collection, and study implementation. This role requires strong communication and organizational skills to manage multiple projects simultaneously.Key Responsibilities:Recruit and coordinate with participants...

Our client is a Medtech startup that seeks to break the notion that physical wellness and exercise is to be enjoyed only by the young. They want to bring physical wellness and rehabilitation to senior folks - enabling them to enjoy the benefits of exercise, but without the stress or strain. Building on the successful launch of their fitness and wellness...

We are currently seeking Clinical Trials Assistant **(**CTA) to join our sponsor-dedicated team in a client facing role. As a vital part of our team, our CTA's perform daily administrative tasks to support to clinical projects and update clinical systems and databases. You will also perform general administrative tasks as needed. You will have excellent...

Company Overview:Parexel International is a leading global biopharmaceutical services company. We are dedicated to providing end-to-end clinical development solutions that meet the needs of our clients.Job Description:The Clinical Trial Assistant will support trial activities during study start-up, conduct, and closeout phases. Key responsibilities include...

About the RoleWe are seeking an experienced Clinical Trials Coordinator to join our team. The successful candidate will be responsible for coordinating all activities related to the operational phase of clinical trials, ensuring timely delivery of quality data while adhering to internal Standard Operating Procedures, applicable laws, and ICH Good Clinical...

Job Summary Medpace is currently looking for full-time Clinical Trial Manager (CTM)in Singapore to lead global clinical research studies. Medpace is a scientifically led organization involved in full services for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. Responsibilities The Clinical Trial...

About the RoleWe are seeking a skilled Clinical Trial Manager to lead our global clinical research studies. As a key member of our team, you will be responsible for overseeing the successful execution of clinical trials from start to finish.Key ResponsibilitiesProvide project leadership for multiservice global clinical trialsInteract with sponsors to ensure...

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience, and level of contribution which they can make to the project. The CTA performs study-related tasks as required by the department,...

About UsOur client is a leading MNC research company in Singapore with specialists, including scientists, doctors, and nurses, who are conducting early phases of trials.Our MissionWe aim to bring new medicine and treatments to improve patient lives.Job OverviewThis role requires the applicant to provide professional care to patients participating in research...

Provides administrative support to project teams in clinical operations in accordance with ICH GCP and local regulations. - Updates and maintains study tracking systems in accordance with the demands of the study e.g. investigational product tracking, payment tracking, CRF tracking, patient tracking, etc - Manages and processes finance-related receipts,...