Clinical Trials Monitoring Manager

Clinical Trials Monitoring Manager RoleThis position is responsible for designing, planning, and conducting clinical research trials by effectively coordinating the activities of study coordinators and investigators and ensuring compliance with study protocols, FDA and International regulations, IRB and/or Ethics committees requirements, and overall clinical...

Roles & ResponsibilitiesAs a Clinical Trials Monitoring Manager, you will design, plan and conduct clinical research trials by effectively coordinating the activities of study coordinators and investigators. This role ensures compliance with study protocols, FDA and International regulations, IRB and/or Ethics committees requirements, and overall clinical...

Roles & ResponsibilitiesJob Overview:We are seeking a highly motivated and detail-oriented Clinical Trial Assistant to join our team. The Clinical Trial Assistant will serve as the unblinded point of contact for logistics vendors and unblinded Clinical Research Associates (CRAs), responsible for managing various aspects of clinical trial logistics and...

Job Summary Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Monitoring team in Singapore. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...

Clinical Trials Monitoring Assistant/ Manager (Global Study Project, Pharma) #HDC Job Description Overview The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the policies and procedures outlined by the Institute and the...

Job Summary Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. 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....

Roles & ResponsibilitiesResponsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager; Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports within the clinical trial management system; ...

Roles & ResponsibilitiesWe are looking for a Manager with sufficient professional experience and stature to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore. The role will mainly assist our Clinical Trials Office to review and finalize contracts related to clinical trials...

Clinical Trials Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1452762 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...

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Monitoring team in Singapore. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise...

Medpace is a leading full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. With over 5,000 employees across 40+ countries, we provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.We are committed to...

Job SummaryThe Clinical Trials Project Specialist will be responsible for planning and executing clinical studies in support of corporate objectives. The ideal candidate will have a strong understanding of clinical study development and execution, with excellent analytical, organizational, and communication skills.Main Responsibilities• Oversee the...

Roles & ResponsibilitiesThe Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials...

We are seeking a skilled Clinical Research Coordinator to support our client in conducting clinical trials in Hematology.The successful candidate will have experience in clinical trials, specializing in Hematology/Oncology interventional trials, and be knowledgeable in setting up cell therapy trials.The ideal candidate will have excellent communication and...

Clinical Trial Project Lead Role SummaryAs a Clinical Trial Project Lead at INSTITUT D'EXPERTISE CLINIQUE SINGAPORE PTE LTD, you will oversee clinical trial projects from initiation to completion, ensuring all phases are executed efficiently and effectively. Key responsibilities include handling various administrative tasks to support project activities...

Clinical Trials Translation Specialist WantedWe are seeking a skilled Clinical Trials Translation Specialist to join our team at ProZ. The ideal candidate will have experience in translating clinical trial documents, including protocols, investigator's brochures, informed consent forms, and chemistry and manufacturing controls.Key Responsibilities:Translate...

Roles & ResponsibilitiesJob Description & Requirements Work closely with the local departments, and adapt to changing priorities with guidance from senior team members. Work with specimens maintained at varying temperatures (ranging from ambient to cryogenic), including the limited movement of shipper boxes filled with dry ice. Perform receipt, QC checks,...

Clinical Trials Project Specialist (Healthcare/ Pharma/ Medical, Regional) The individual in this position will participate on multi-disciplinary project teams to plan and execute successful clinical studies in support of corporate objectives. The Clinical Trial Manager will demonstrate proficiency in all areas of clinical study development and execution,...

We are seeking an experienced Clinical Trials translator to work on our projects in Singapore. As a key member of our team, you will be responsible for translating clinical trial documents from English to Brazilian Portuguese.Job Description:We are looking for qualified translators with expertise in the pharmaceutical industry, particularly in Clinical...

Clinical Trials Translation and Editing ServicesWe are seeking qualified English to Greek freelancers to work on our Clinical Trials related Projects. The ideal candidate will have experience in translation and editing of clinical documents, including protocols, investigator's brochures, informed consent forms, and chemistry and manufacturing...