Clinical Study Start Up Associate

About the RoleAt ICON, we're committed to advancing and improving patients' lives through clinical research. As a Study Start Up Associate, you'll play a vital role in ensuring that physicians at our research sites are prepared to start clinical trials.Key Responsibilities:Coordinate and facilitate activities related to the completion of Critical Document...

About ICONAt ICON, we pride ourselves on being a diverse and dynamic organization that enables us to deliver excellence to our clients and patients. Our 'Own It' culture is built on four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. We strive to be the Clinical Research Organisation of choice in drug development.We're...

Study Start Up Associate IIAt Icon, we are seeking a highly skilled Study Start Up Associate II to join our team. As a key member of our study start up team, you will be responsible for collecting, preparing, reviewing, approving, processing, and tracking regulatory and site-level critical documents required for study site activation.Key...

About the Role:As a Study Start Up Manager at ICON Plc, you will play a critical role in ensuring the successful preparation, review, and approval of study master, country-related, and site-level informed consent documents. Your expertise in clinical research operations will be instrumental in coordinating and leading a team of Study Start Up Associates,...

Job SummaryWe are seeking a highly skilled and detail-oriented Study Start Up Associate I to join our team at ICON Plc. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesCoordinate and facilitate activities related to the...

About ICONAt ICON, our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.As a world-leading healthcare intelligence and clinical research organization, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and...

Job SummaryWe are seeking a highly skilled Study Start Up Associate I to join our team at Icon. As a key member of our study start up team, you will be responsible for ensuring the successful activation of study sites in accordance with Icon SOPs, Sponsor SOPs, and applicable country regulations.Key ResponsibilitiesRegulatory Document ManagementCollect,...

Job SummaryICON is seeking a highly skilled Study Start Up Associate I to join our team in Mexico City. As a Study Start Up Associate I, you will play a critical role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key...

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 fulfill 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,...

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 fulfill 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 organization: Accountability & Delivery, Collaboration,...

About the RoleAt ICON, we're committed to advancing and improving patients' lives through clinical research. As a Study Start Up Associate II, you'll play a critical role in ensuring that our research sites are prepared to start clinical trials of investigational products.Key ResponsibilitiesReview and negotiate clinical site investigator contracts and...

About the RoleAs a Study Start Up Manager at ICON, you will play a critical role in leading a global team of Study Start Up Associates. Your primary responsibility will be to coordinate and facilitate the activities related to preparation, review, and approval of Study Master, country-related, and site-level Informed Consent documents in accordance with...

Key Responsibilities:1. Resource Management: Oversee the allocation of resources to ensure efficient delivery of line management training and functional delivery within the Study Start Up Operations group.2. Line Management: Provide guidance and support to line managers to enhance their skills and abilities in training and functional delivery.3. Quality...

**Job Summary:**The Clinical Study Coordinator will play a critical role in the conduct of clinical research studies at Avantgarde Human Capital Consultants. This position will support the site's Principal Investigator in the development, monitoring, implementation, and closeout of assigned protocols.**Key Responsibilities:**• Develop and maintain a...

About the RoleWe are seeking a highly skilled and motivated Clinical Trial Associate to join our team at ICON. As a Clinical Trial Associate, you will play a critical role in the success of our clinical trials by providing administrative support to our project teams.Key ResponsibilitiesAssist project teams with the set-up, organization, and maintenance of...

Job OverviewAs a Clinical Research Associate at Novasyte, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to conduct site monitoring visits to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, and...

About the RoleThe Clinical Project Manager (CPM) is a key member of the Global Drug Development team at Novartis, responsible for the planning, execution, and reporting of assigned studies in assigned geographies. The CPM serves as the single point of contact and study team lead, ensuring aligned communication with Trial Lead and other Clinical Trial Team...

Job SummaryThe Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. This role oversees the clinical portion of the budget, develops monitoring plans and tools, trains clinical research associates, drives enrollment and study start-up activities, reviews trip reports, implements corrective and preventative action plans,...

Job SummaryAt ICON Plc, we are seeking a highly skilled Clinical Associate to join our team. As a Clinical Associate, you will be an integral part of the study team, responsible for tracking and maintaining study activities, and ensuring global inspection readiness.Key ResponsibilitiesProvide administrative support to the Project Manager(s), Clinical Trial...

About the RoleWe are seeking a highly motivated and organized Clinical Trial Associate to join our team at ICON. As a Clinical Trial Associate, you will play a critical role in the success of our clinical trials.Key ResponsibilitiesAssist project teams with the set-up, organization, and maintenance of clinical study documentation, including preparation for...