Clinical Trial Manager

hace 5 meses


Santiago de Chile ICON plc A tiempo completo

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip reports, implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities. The CTM will also participate in Sponsor, Investigator and bid defense meetings. You will need: - 4 year degree or equivalent combination of education & experience - Demonstrated ability to drive the clinical deliverables of a study - Subject matter expertise in the designated therapeutic area - Prior monitoring experience is preferred - Ability to travel up to 20% - Fluent in local language - both written & verbal Benefits of Working in ICON: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know



  • Santiago, Chile IQVIA A tiempo completo

    Clinical Trial Manager – Sponsor Dedicated. Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operations deliverables progress according to agree upon...

  • Clinical Trial Manager

    hace 5 meses


    Santiago de Chile ICON plc A tiempo completo

    At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

  • Clinical Trial Coord

    hace 5 meses


    Santiago de Chile Thermo Fisher Scientific A tiempo completo

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving...


  • Santiago de Chile CTI Clinical Trial Services, Inc A tiempo completo

    **Senior Clinical Research Associate** **(Level dependent on experience)** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can...


  • Santiago de Chile CTI Clinical Trial Services, Inc A tiempo completo

    **Senior Clinical Research Associate** (Level dependent on experience)** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can...


  • Santiago, Metropolitana, Chile Thermo Fisher Scientific A tiempo completo

    Job SummaryWe are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. As a Clinical Trial Coordinator, you will play a critical role in the successful execution of clinical trials, ensuring that all tasks are completed on time, within budget, and to a high-quality standard.Key...


  • Santiago, Metropolitana, Chile Thermo Fisher Scientific A tiempo completo

    Job SummaryAs a Clinical Trial Coordinator at Thermo Fisher Scientific, you will play a vital role in ensuring the smooth operation of clinical trials. Your primary responsibility will be to perform department, internal, country, and investigator file reviews as assigned and document findings in the appropriate system. You will also be responsible for...

  • Clinical Associate

    hace 5 meses


    Santiago de Chile ICON plc A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...


  • Santiago, Metropolitana, Chile Thermo Fisher Scientific A tiempo completo

    {"title": "Clinical Trial Coordinator", "description": "Key ResponsibilitiesAs a Clinical Trial Coordinator at Thermo Fisher Scientific, you will be responsible for ensuring the smooth execution of clinical trials. Your key responsibilities will include:Performing department, internal, country, and investigator file reviews as assigned and documenting...


  • Santiago de Chile Fortrea A tiempo completo

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

  • Clinical Trial Coord

    hace 5 meses


    Santiago de Chile Thermo Fisher Scientific A tiempo completo

    Clinical Trial Coordinator: Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization's SOPs and department guidance documents. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate...


  • Santiago de Chile MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary...

  • Clinical Trial Coord

    hace 6 meses


    Santiago de Chile Thermo Fisher Scientific A tiempo completo

    According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s). - Ensures allocated tasks are performed on time, within budget and...


  • Santiago, Metropolitana, Chile Thermo Fisher Scientific A tiempo completo

    Job SummaryThermo Fisher Scientific is seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team. As a Clinical Trial Coordinator, you will play a critical role in the success of our clinical trials by ensuring timely and accurate completion of tasks, maintaining high-quality standards, and providing exceptional support to...


  • Santiago de Chile MSD A tiempo completo

    **Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally....

  • Prin Cra

    hace 7 meses


    Santiago de Chile Thermo Fisher Scientific A tiempo completo

    Monitors investigator sites with particular ability to manage complex studies and/or challenging sites using a risk-based monitoring approach, applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data...


  • Santiago de Chile Novasyte A tiempo completo

    Unleash Your Potential It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward. Join IQVIA and see where...


  • Santiago, Chile CDS Fortrea Inc. A tiempo completo

    As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...


  • Santiago de Chile MSD A tiempo completo

    The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary...


  • Santiago de Chile Grifols Chile SA A tiempo completo

    Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic,...