Clinical Trials Manager

**Job Description:**Jobscentral is seeking a Clinical Trials Coordinator to join our team. As a Clinical Trials Coordinator, you will be responsible for ensuring the smooth operation of clinical trials, including specimen identification, processing, and storage.You will work closely with the laboratory team to ensure that all test results meet high standards...

ResponsibilitiesThe primary responsibility of this role is to educate and demonstrate the benefits of our key products to clinical professors, teaching-hospital faculty, residents, and students.This will involve providing medical information to internal and external health sources, exploring and identifying sites for clinical trials in all stages of...

Job 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, and...

About This OpportunityThis is an exciting opportunity to join our team as a Clinical Associate and contribute to our research efforts. As a Clinical Associate, you will work closely with our research team to support the conduct of clinical trials and other research projects. You will have the opportunity to gain valuable experience in research methodology,...

Position SummaryWe are seeking a detail-oriented Clinical Trials Assistant to support our clinical research team. In this role, you will assist in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports. You will also be responsible for managing case report forms, queries, and clinical data flow. If you have...

We are looking for an Assistant Project Manager / Project Team Lead for the Division of Clinical Trials & Epidemiological Sciences - Clinical Trials Office (CTE-CTO) within NCCS. This role will manage multi-site investigator-initiated trials (IITs) from start-up to close-out. The role is required to liaise with multiple stakeholders to set up the IITs and...

Roles & ResponsibilitiesThe Role: In this role, the candidate will provide an enhanced level of customer support and operational support for movement of any cell and gene shipment through the Company’s logistics network. You will work with our global depot facilities and branches and a cross functional team to transition new studies, facilitate these...

Roles & ResponsibilitiesThe Role: In this role, the candidate will provide an enhanced level of customer support and operational support for movement of any cell and gene shipment through the Company’s logistics network. You will work with our global depot facilities and branches and a cross functional team to transition new studies, facilitate these...

Roles & ResponsibilitiesResponsibilitiesProvide day-to-day departmental/project support activities, such as managing study supply inventory and orders, shipping, filing, faxing, etc.; Coordinate and provide minutes for department/project meetings or conference calls; Conduct quality review of documents; Maintain databases/spreadsheets and compile reports;...

Roles & ResponsibilitiesInterested applicants are invited to apply directly at the NUS Career PortalYour application will be processed only if you apply via NUS Career PortalWe regret that only shortlisted candidates will be notified.Job SummaryWe are seeking a Master’s/PhD level Clinical Trials Biostatistician to support the design, analysis, and...

OverviewMEDPACE IS A GLOBAL LEADER IN CLINICAL CONTRACT RESEARCH ORGANIZATION SERVICES. WE PROVIDE PHASE I-IV CLINICAL DEVELOPMENT SERVICES TO THE BIOTECHNOLOGY, PHARMACEUTICAL AND MEDICAL DEVICE INDUSTRIES. OUR MISSION IS TO ACCELERATE THE GLOBAL DEVELOPMENT OF SAFE AND EFFECTIVE MEDICAL THERAPEUTICS THROUGH OUR SCIENTIFIC AND DISCIPLINED APPROACH.Job...

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 include: ...

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 include: ...

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...

We are seeking a highly motivated and organized Research Assistant to join our team. As a research assistant, you will assist in the coordination and execution of clinical trials, including patient recruitment and retention, data management, and regulatory compliance.The ideal candidate will have a strong foundation in research methods and procedures, with...

Job RoleThe Clinical Trials Assistant will be responsible for providing support to the clinical research team in the maintenance of clinical documents and systems. Key responsibilities include: Main ResponsibilitiesMaintaining accurate and up-to-date clinical documents and systems.Preparing, handling, distributing, filing, and archiving clinical...

Roles & ResponsibilitiesJob Title: Operation AssociateSalary: Up to $2,800/monthWorking Hours: 8:00 AM - 5:00 PM (Monday - Friday)Job Description:Join a global leader in drug delivery technology and development solutions for pharmaceutical products. We are seeking a dedicated and meticulous Operation Associate to perform key operational processes in the...

Key Responsibilities:The Medical Lead will be responsible for ensuring that medical enquiries are responded to in a high quality, timely manner and in accordance with applicable standards. This includes establishing standard response documents as appropriate, for frequently asked questions. The Medical Lead will also provide medical/scientific input into the...

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...