100+ Clinical Trials Jobs - June 2026 - High Salaries

显示102个工作的结果 "clinical trials"

不要错过任何 Clinical Trials 的新工作机会

MYR4,000 - MYR7,500 每月

Bandar Kuala Lumpur, WP Kuala Lumpur

靠近火车站
  • Assist doctors during examinations, procedures, and emergencies
  • Maintain proper documentation of patient records and nursing notes
  • Ensure adherence to hospital policies, infection control, and safety standards ...
Posted
a month ago
Undisclosed

Singapore

  • Evaluation and validation of new assessment methods for implementation in clinical studies
  • Contribute to the establishment of global standards for gerotherapeutic trials and international clinical trial networks
  • Oversee the execution of clinical trials, ensuring adherence to protocols, standard operating procedures (SOPs), and good clinical practice (GCP) ...
Posted
11 days ago
Undisclosed

Singapore

  • Evaluation and validation of new assessment methods for implementation in clinical studies
  • Contribute to the establishment of global standards for gerotherapeutic trials and international clinical trial networks
  • Oversee the execution of clinical trials, ensuring adherence to protocols, standard operating procedures (SOPs), and good clinical practice (GCP) ...
Posted
11 days ago
SGD2,500 - SGD3,500 每月

Islandwide (Singapore)

  • ·        To provide administrative and secretarial supportto research projects, such as organizing regular meetings to maintain regularcommunication with other members of the research team and procurement ofmaterials.
  • ·        To assist clinical study database formation,data collection.
  • Requirements ...
Posted
23 days ago
Undisclosed

Singapore

  • Evaluation and validation of new assessment methods for implementation in clinical studies
  • Contribute to the establishment of global standards for gerotherapeutic trials and international clinical trial networks
  • Oversee the execution of clinical trials, ensuring adherence to protocols, standard operating procedures (SOPs), and good clinical practice (GCP) ...
Posted
22 days ago
Undisclosed

Singapore

  • Introduction and improvement of biological, clinical, and digital biomarkers of aging into clinical trial protocols with a specific focus on markers of NAD+ metabolism and mitochondrial function.
  • Lead the innovation of NAD+ precursors and generate the evidence for their potential use in precision geromedicine
  • Contribute to the establishment of global standards for gerotherapeutic trials and international clinical trial networks ...
Posted
a month ago
Undisclosed

Singapore

  • Introduction and improvement of biological, clinical, and digital biomarkers of aging into clinical trial protocols with a specific focus on markers of NAD+ metabolism and mitochondrial function.
  • Lead the innovation of NAD+ precursors and generate the evidence for their potential use in precision geromedicine
  • Contribute to the establishment of global standards for gerotherapeutic trials and international clinical trial networks ...
Posted
a month ago
Undisclosed

Kwai Tsing District

  • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. ...
Posted
a month ago
Undisclosed

Singapore

  • Precision Health Research, Singapore (PRECISE)
  • Singapore Translational Cancer Consortium (STCC)
  • Cardiovascular Disease National Collaborative Enterprise (CADENCE) ...
Posted
a month ago
Undisclosed

Singapore

  • Precision Health Research, Singapore (PRECISE)
  • Singapore Translational Cancer Consortium (STCC)
  • Cardiovascular Disease National Collaborative Enterprise (CADENCE) ...
Posted
a month ago
Undisclosed

Singapore

  • Characterize and evaluate electromechanical properties of soft systems.
  • Use simulation tools for design and modeling.
  • Implement and test developed devices for various applications. ...
Posted
11 days ago

Research Associate/Fellow (Clinical Trials - Healthy Longevity)

Undisclosed

Singapore

  • Published in reputable international journals.
  • Responsible and able to work independently.
  • Good written and spoken communication. ...
Posted
16 days ago
Undisclosed
WFH

Singapore

  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
  • Develop operational project plans; ...
Posted
2 days ago
Undisclosed

Singapore

  • Accurate planning and co-ordination of operational feasibility of trial timelines for their R/OPU; and oversight of trial preparation to ensure trial team members are aligned and on track.
  • Verifies and provides input into the country and site level feasibility and OPU commitment (site and patient commitment). Finalize and validate site selection using available data sources and local insights/expertise, in collaboration with other functions (i.e. Medical Affairs, vendors if applicable).
  • Development and implementation of country level engagement plans, recruitment planning and risk mitigation. Co-ordinates development of country level patient facing documents in close collaboration with relevant internal and external stakeholders. Reports patient and site level feedback as strategic insight to contribute to improving trial design with a focus on patient value. ...
Posted
16 days ago
Undisclosed

Singapore

  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
  • Develop operational project plans; ...
Posted
19 days ago
SGD5,000 - SGD5,000 每月

Singapore

  • Supervise and provide advice to the executives of the Feasibility Team in NDA negotiation and to act as back-up for such review and negotiation during manpower shortage.
  • Assist in approving online payments in APIMS, training applications in People’s Connexion and any other online applications assigned.
  • Help to oversee financial and insurance reporting to CTCC as well as annual NMRC reporting. ...
Posted
16 days ago
Undisclosed

Singapore

  • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. ...
Posted
18 hours ago
SGD4,500 - SGD4,500 每月

Singapore

  • The National University of Singapore (NUS) is recruiting a full-time Research Associate at the ADVANcing Clinical Evidence in Infectious Diseases (ADVANCE-ID) Network, Saw Swee Hock School of Public Health (SSHSPH). Founded in 1905, NUS is consistently ranked among the world's top 30 universities and Asia's top 2 universities. It is an innovative, research-intensive university with over 36,000 students from 100 countries. ADVANCE-ID is a global network for infectious disease clinical studies. Our aim is to conduct rapid, cost-effective randomised controlled trials to deliver relevant and high-quality evidence to guide clinical practice. We hope to achieve this vision through equity (shared ownership), sustainability (build long-term capacity and trust) and engagement of key stakeholders (including clinicians, scientists, governments, industry).
  • We are seeking a highly organized and proactive Research Associate with strong project management expertise to support a regional initiative that aims to develop and evaluate community engagement strategies in clinical trials. This role involves end-to-end project management as the primary focus and will also support research activities. This position will work closely with principal investigators, country leads and research teams, and external partners to drive operational excellence, compliance, and impact.
  • Job scope:• Project management: planning, communication, coordination, timeline management, monitoring, and budget, data and resource management• Stakeholder and partner management and serve as the central point of contact among stakeholders• Organize cross-country meetings; prepare agendas and minutes.• Coordinate travel and support site visits; travel to participating countries as needed.• To work with the lead investigator on collaborative and international research with partner organisations nationally and globally (including NGOs, industry, hospitals and other research and academic institutions).• Assist research activities as needed, including qualitative and quantitative research data collection, analyses, and reporting.• Prepare and coordinate research ethics protocols.• Support the dissemination of project outcomes through appropriate channels and outlets including guidelines and policy recommendations.• Be involved in capacity building in the region by supporting workshops and relevant training activities. ...
Posted
9 days ago
Undisclosed

Singapore

  • Organize cross-country meetings; prepare agendas and minutes.
  • Coordinate travel and support site visits; travel to participating countries as needed.
  • To work with the lead investigator on collaborative and international research with partner organisations nationally and globally (including NGOs, industry, hospitals and other research and academic institutions). ...
Posted
11 days ago
Undisclosed

Singapore

  • Coordinate travel and support site visits; travel to participating countries as needed.
  • To work with the lead investigator on collaborative and international research with partner organisations nationally and globally (including NGOs, industry, hospitals and other research and academic institutions).
  • Assist research activities as needed, including qualitative and quantitative research data collection, analyses, and reporting. ...
Posted
13 days ago
Undisclosed
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. ...
Posted
20 days ago
Undisclosed
  • Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
  • Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
  • Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. ...
Posted
20 days ago
Undisclosed
WFH

Singapore

  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
  • Develop operational project plans; ...
Posted
2 days ago
SGD3,500 - SGD3,500 每月

Singapore

  • ·        Ensure safety and well-being of study subjects, andall clinical trial data are reliable
  • ·        Recognise emergency situations and assist intreatment procedures
  • ·        Prepare research metrics and reports forsubmission ...
Posted
6 days ago
Undisclosed

信義區

  • Coordinate and verify changes to the database and application using appropriate change control procedures and ensure comprehensive and accurate documentation is completed.
  • Act as off-hours escalation point for junior IWRS Clinical Monitor resources or the outsourced call centre service to resolve high urgency client requests (based on agreed rotational schedule amongst IWRS Clinical Trials Monitor resources).
  • Generate, maintain, and/or review CTT Requirements Specification documents. ...
Posted
11 days ago
Undisclosed

信義區

  • Responsible for set-up, maintenance, and archival of studies in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
  • Establish, maintain, and archive files of essential documents from investigative sites and for inclusion in TMF. These files must be maintained in a fashion so that they are continuously available for inspection and completion for archive.
  • Assist with site identification, feasibility questionnaire development and distribution, and site selection. ...
Posted
12 days ago
SGD3,500 - SGD3,500 每月

Singapore

  • ·        Ensure safety and well-being of study subjects, andall clinical trial data are reliable
  • ·        Recognise emergency situations and assist intreatment procedures
  • ·        Prepare research metrics and reports forsubmission ...
Posted
12 days ago
Undisclosed
WFH

Singapore

  • Interact with the internal project team, Sponsor, study sites, and third-party vendors;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Provide oversight and management of study supplies; ...
Posted
2 days ago
Undisclosed
WFH

Singapore

  • Interact with the internal project team, Sponsor, study sites, and third-party vendors;
  • Provide oversight and quality control of our internal regulatory filing system;
  • Provide oversight and management of study supplies; ...
Posted
2 days ago