Empleos de IRE en México

As a Clinical Operations Manager at ICON, you'll work ensure delivery and development of the Clinical Operations team against key metrics. Work with Leadership to develop and grow capabilities, productivity, and quality. · ...

We are currently seeking a Pharmacovigilance Assistant I to join our diverse and dynamic team. · ...

We have an opportunity for a Clinical Data Coordinator II to join ICON's Full Service IOD Clinical Data Science team. The CDC II supports and executes the data review activities, including data validation and analytics, that contribute to delivery of clinical data that meets agre ...

This role involves supporting site partners in collecting, reviewing, organizing and assembling initial start-up packages for clinical trials. · ...

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.What You Will Be Doing: · Coordinating monitoring activities at clinical trial sites. · ...

We are currently seeking a Senior Manager, Pharmacovigilance to join our diverse and dynamic team. · Degree in life sciences, pharmacy, or a related field; advanced degree or relevant certifications are preferred. · Significant experience in pharmacovigilance or drug safety, idea ...

Collect outstanding invoices for several ICON Business Units. · Fluency in English. · 2+ years of experience in collections, accounts receivable, or related financial roles. · ...

Job summary · ICON plc is seeking a Contract Analyst I to join their team in Mexico City. The role involves preparing and verifying invoices for assigned accounts and interacting closely with the Revenue team to ensure timely billing. · ...

We are seeking a highly skilled Business Continuity Manager to join our team and help ensure ICON is prepared to respond effectively to business interruptions. · ...

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. · ...

We are seeking a Site Management Associate I to support the management of clinical trial sites by assisting with site monitoring activities and ensuring compliance with study protocols. · We're proud to foster an inclusive environment driving innovation and excellence at ICON plc ...

We are seeking a Clinical Supplies Senior Manager to join our team. As a Senior Manager you will oversee the planning procurement and distribution of clinical supplies ensuring smooth execution of clinical trials.As a member of our diverse and dynamic team you will be instrumenta ...

ICON plc is seeking a Site Management Associate II to join their team in Mexico City. The role involves coordinating monitoring activities at clinical trial sites and ensuring compliance with study protocols. · Coordinating monitoring activities at clinical trial sites. · Assisti ...

Senior Regulatory Technician at ICON plc in Mexico City. The job involves working with the Clinical Trials Information System (CTIS), providing support for submissions and other documents by performing necessary tasks. · ...

We are currently seeking a Senior Clinical Data Science Programmer to join our diverse and dynamic team. · Developing, validating, and maintaining programming solutions for data analysis and reporting in clinical trials. · Collaborating with clinical data scientists and biostatis ...

We are currently seeking a Data Monitoring Committee Specialist to join our diverse and dynamic team. As a Project Leader at ICON, you will be responsible for guiding and managing project teams to ensure the successful delivery of projects. ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · ...

+Job summary · We are currently seeking a Clinical Supplies, Senior Manager Management to join our diverse and dynamic team.Leading and managing the clinical supplies team, overseeing the procurement, storage, and distribution of clinical trial materials to ensure timely and accu ...

We are currently seeking a Trial Master File Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for overseeing the Trial Master File (TMF) management processes, ensuring compliance with regulatory requirements and best practices in clinical ...

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. · ...