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ICON

Empleos de ICON en México

365 trabajos de ICON en México


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    Job Overview: · Our client seeks a Clinical Payment Associate to collaborate with the CP&P team and other departments, such as local and global clinical teams and finance, to obtain necessary information required to configure the CTPS and resolve escalated issues. · Key Responsib ...


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    ICON plc is a world-leading healthcare intelligence and clinical research organization. · We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government organizations. · Our patients are at the center of all we do, ac ...


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    Senior Clinical Scientist Role · Join a world-leading clinical research organisation and make a difference in healthcare intelligence. · The Regional Clinical Scientist will collaborate with the Study Medical Monitor/Study Clinical Scientist to provide scientific and clinical sup ...


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    As an Account Growth Manager at ICON, you will be responsible for proactively identifying and pursuing sales opportunities within assigned territories or accounts. You will engage with potential clients to understand their needs, provide product information, and offer tailored so ...


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    Job Description** · As a Research Site Partner Coordinator, you will play a key role in facilitating the relationship between our company and clinical trial investigators and research site staff. · Your primary responsibility will be to develop and maintain strong relationships w ...


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    About You · To succeed in this role, you'll need a strong analytical mindset, excellent problem-solving skills, and the ability to interpret complex data. · You should possess advanced English proficiency, with prior experience in contract analysis, finance, or a related field be ...


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    Your Role · Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes. · Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in ...


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    What You Will Do · In this role, you will oversee local vendor selection and performance as needed, while ensuring adherence to financial standards, prevailing legislation, ICH/GCP, IRB/IEC, Health Authority and SOP requirements. · Main Responsibilities: · Leads all SSU activitie ...


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    Company Overview · At ICON, our people are the driving force behind our success. A diverse team of talented professionals enables us to become a better partner to our clients and helps us achieve our mission to advance and improve patients' lives. · We operate under an 'Own It' c ...


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    Welcome to ICON, where our diverse teams enable us to become a better partner to our customers and help fulfill our mission to advance patients' lives. · Our culture is built on four key values that bring us together as individuals and set us apart as an organisation: Accountabil ...

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    Cta

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    Job Summary · As a Clinical Trial Associate, you will be working with the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. · Key Responsibilities · Assists in the coordination and administration of study activities from st ...


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    About ICON plc · We are a world-leading healthcare intelligence and clinical research organisation, advancing clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. · Our patients are at ...


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    Job Overview · We are seeking a highly skilled Regulatory Data Coordinator to join our team at ICON. This role will involve managing, maintaining, and organizing regulatory data to ensure compliance with global standards. · About the Role · The successful candidate will be respon ...


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    At ICON, you will be joining a world-leading clinical research organization that delivers healthcare intelligence and unparalleled expertise. As our ideal candidate, you will contribute to the success of our team by overseeing the quality and completeness of trial documents. · Ab ...


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    Job Description · About the Role: As a Clinical Data Science Lead, you will be joining our team to lead effectively under pressure, demonstrating agility and innovation in team leadership. You will be responsible for supporting the design, specifications, and development of eCRFs ...


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    Job Summary · \The Clinical Data Science Lead is responsible for leading end-to-end data review activities on clinical trials. This involves partnering with cross-functional teams to develop and implement strategies for ensuring the accuracy and integrity of clinical trial data. ...


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    Role Overview · The Study Start-Up Manager is accountable for study planning, SSU activities and activation deliverables of assigned projects in compliance with client processes, GCP/ICH and regulatory requirements in a standalone country, OPC (operating country) or satellite cou ...


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    At ICON, our diverse teams enable us to become a better partner to our customers and advance patient care. · We're driven by four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. Our goal is to deliver excellence in clinical research. · We're look ...


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    **Who We Are** · ICON plc is a global leader in healthcare intelligence and clinical research. Our diverse teams enable us to deliver high-quality services to our customers and achieve our mission to advance and improve patients' lives. · **The Job** · This role supports the Proj ...


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    At ICON, our people are what set us apart. · Our diverse teams enable us to become a better partner to our customers and help us fulfill our mission to advance and improve patients' lives. · Role Overview · We are looking for an Administrative Assistant to join our team. · This r ...