Empleos de ICON plc en México

As a Senior Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also provide support for submissions and other documents by performing necessary tasks including assembly, dispatch among others and coordinating resources for submissions ...

We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. · We will contribute to ensuring the safety and efficacy of therapies by assisting in the collection, analysis, · and communication of safety data in compliance with regulatory r ...

+ Resource Planning Specialist - Mexico ICON plc is a world-leading healthcare intelligence and clinical research organization We're proud to foster an inclusive environment driving innovation and excellence , as well as collaborate effectively across teams and influence stakehol ...

We're proud to foster an inclusive environment driving innovation and excellence, · Support collection and assembling of all documents needed in the Critical Document Package (CDP) and/or those required for site activation, · Acurate forecast Site Activation plans · ...

Clinical Data Coordinator · This is a hybrid role combining on-site collaboration with remote work flexibility. · Main responsibilities include assisting Study Leads with eCRF maintenance, · clinical data reconciliation based on edit specifications · tracking task metrics for pro ...

We are currently seeking a Project Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities... · ...

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. · As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, · ensuring c ...

We are currently seeking a Manager Quality Assurance to join our diverse and dynamic team. As a Manager Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, · Developing and implementing quality assurance strategies an ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · The Senior Clinical Data Science Lead (Senior CDSL) serves as the primary contact for internal and externa ...

+Job summary · +Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements. Participate in the identification and resolution of data discrepancies and issues, working to streamline data flow and en ...

We're proud to foster an inclusive environment driving innovation and excellence, · The Collections Specialist is responsible for collecting outstanding invoices and building strong relationships with clients. · , · Manage Accounts Receivable ledger · ,Ensure timely payments from ...

ICON plc is a world-leading healthcare intelligence and clinical research organization. · ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Maintain applicable study-level account access for assigned projects for CTIS to maintain compliance and c ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Various annual leave entitlements A range of health insurance offerings to suit you and your family's need ...

We are currently seeking a Resource Planning Specialist to join our diverse and dynamic team. As a Resource Planning Specialist at ICON plc you will play a key role in supporting project risk management efforts by assisting with data collection analysis and reporting. · Bachelor' ...

We are seeking a Site Management Associate II to support the management and monitoring of clinical trial sites by ensuring compliance with study protocols and regulatory requirements.Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols ...

As Clinical Data Coordinator II at ICON PLC you will be assisting in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. · Manage clinical and third-party data reconciliation based on edit specifications and data review plans. · Tracks and communic ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · ...

We are currently seeking a Director Quality Assurance to join our diverse and dynamic team. As a Director Quality Assurance at ICON, you will play a pivotal role in ensuring the quality and compliance of clinical trials, · Leading the development and implementation of quality ass ...

ICON plc is a world-leading healthcare intelligence and clinical research organization. · We are seeking a Clinical Scientist to join our diverse and dynamic team. · Clinical Scientists at ICON play a pivotal role in designing and conducting clinical studies that evaluate the saf ...