Clinical trials associate

3 days ago


Singapore IQVIA LLC Full time

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 therapies at the country level, and be the liaison between the site and Contract Research Organization (CRO) / Pharmaceutical Company. Learning Opportunities: Participate in comprehensive Good Clinical Practice (GCP) Training: Setting you up for success in Clinical Research Gain knowledge in Clinical Research Industry, Ethics in Clinical Research, Fundamentals of Good Clinical Practice Training, Regulatory Inspection Readiness, Clinical Trial Management System, and Introduction to electronic Trial Master File Understand Site Activation such as the process of starting up a clinical trial in Singapore, finding the right investigators for a clinical trial in Singapore, regulatory documents collection, review, approval and maintenance of clinical trials regulatory documents Perform tasks assigned by a manager in either the site activation or site management department, supplemented by soft skills trainings and technical trainings (Trainings may Include: Effective Minute taking during Meetings, Managing Challenging Communications, Cross-cultural Awareness) Key Requirements: Bachelor of Science in Life Sciences or Healthcare, Biosciences, Pharmacy related disciplines. Good interpersonal communication and organizational skills Good written and verbal communication skills including good command of English Good word processing skills and knowledge of MS Office applications Good attention to detail General awareness of clinical trial environment and drug development process Ability to establish and maintain effective working relationships with co-workers, managers and sponsors IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. #J-18808-Ljbffr



  • Singapore IQVIA LLC Full time

    Clinical Trials Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1452762This 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...


  • Singapore PRESTIGE BIOPHARMA LIMITED Full time

    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...


  • Singapore RECRUIT EXPRESS PTE LTD Full time

    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...


  • Singapore MEDPACE SINGAPORE PTE. LTD. Full time

    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; ...


  • Singapore RECRUIT EXPRESS PTE LTD Full time

    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...


  • Singapore MEDPACE Full time

    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...


  • Singapore NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD Full time

    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...


  • Singapore Medpace, Inc. Full time

    Job Summary Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (a CTM) to join our Clinical Trial Management team in Singapore. The a CTM will be a part of the Clinical Trial Management team working with...


  • Singapore NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD Full time

    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...


  • Singapore Bancroft School Full time

    Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (a CTM) to join our Clinical Trial Management team in our Singapore office. The a CTM will be a part of the Clinical Trial Management team and support Project Coordinators...


  • Singapore GMP TECHNOLOGIES (S) PTE LTD Full time

    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...


  • Singapore Medpace, Inc. Full time

    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....


  • Singapore ProZ Full time

    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...


  • Singapore INSTITUT D'EXPERTISE CLINIQUE SINGAPORE PTE LTD Full time

    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...


  • Singapore RECRUIT EXPRESS PTE LTD Full time

    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...


  • Singapore Bancroft School Full time

    Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (a CTM) to join our Clinical Trial Management team in Singapore. The a CTM will be a part of the Clinical Trial Management team working with Project...


  • Singapore Recruit Express Pte Ltd. Full time

    Clinical Trials Management Affiliate (Pharmaceutical MNC, Regional) Singapore | Posted: Nov 06, 2024 Job Description As a CTM, you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes, adding value to our business and meeting client needs. Primary point of contact for...


  • Singapore ProZ Full time

    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...


  • Singapore ProZ Full time

    Clinical Trials Translation and Editing OpportunityJob posted at: Our Singapore location (GMT: )Job type: Translation/editing/proofing jobServices required: Translation, Checking/editingJob Description:We are seeking a qualified Clinical Trials Translation Specialist for our projects in Singapore. As a member of our team, you will be responsible for...


  • Singapore PRESTIGE BIOPHARMA LIMITED Full time

    Roles & ResponsibilitiesJob Description & RequirementsJob Description Protocol Review: Review and understand the study protocol, which outlines the objectives, design, methodology, and conduct of the clinical trial. Site Selection: Participate in the selection of appropriate clinical trial sites and investigators based on their qualifications and ability...