Regulatory Submission Manager - Ciudad de México

The Regulatory Submission Manager is responsible for managing end-to-end regulatory lifecycle submissions across multiple markets. · The role coordinates with cross-functional teams to execute lifecycle management activities, · maintains regulatory compliance, · and supports GSK' ...

This role will provide YOU the opportunity to lead key activities to progress YOUR career. · Own end‑to‑end delivery of assigned complex lifecycle regulatory submissions (e.g., variations, PBRERs, renewals, site registrations/renewals, tenders, etc.), ensuring they meet agency re ...

We are seeking a Manager, Regulatory Affairs to join our diverse and dynamic team. You will play a pivotal role in contributing to drug development as part of the Regulatory Affairs team. · Lead regulatory activities and submissions independently. · Provide regulatory guidance an ...

+We are currently seeking a Manager, Regulatory Affairs to join our diverse and dynamic team. · +Lead regulatory activities and submissions independently, with prior experience in areas such as CTA/IND/MAA. · +Provide regulatory guidance and efforts to internal teams. · +Particip ...

Astellas' Global Capability Centres – Overview Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. · ...

Job summary · We are seeking a Senior Translations Project Manager to coordinate and manage Regulatory Submissions translation/localization projects from receipt to completion. · ...

Coordinate and manage the full lifecycle of Regulatory Submissions translation and localization projects for Marketing Authorization. · ...

We're looking for a Regulatory Affairs Manager to join our team in Mexico City. You will play a critical role in coordinating regulatory submissions and providing regulatory expertise to labeling changes. · Responsible for coordinating regulatory submissions sent to the distribut ...

Join Medpace at our Mexico City office as a Regulatory Submissions Coordinator. The role involves working within Regulatory Submissions, supporting projects and gaining experience in study start up. · ...

Join Medpace at our Mexico City office As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions supporting our many projects and gaining vital experience in study start up You will be a productive member of the team and will be m ...

We are looking for a Legal Directory Specialist (LDS) to lead the end-to-end management of legal directories and rankings · (Chambers & Partners, The Legal 500, IFLR, Leaders League, among others). This role is pivotal to strengthening the visibility and reputation of firms and l ...

This is a Regulatory Affairs professional with local/regional responsibility. · ...

We are looking for a Start-Up Specialist to join our team and make a difference in the execution of study start-up activities. · ...

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:Bachelor's degree in pharmacy, chemistry, biotechnology or a related field. · Strong understanding of regulatory submission requirements and lifecycle management proces ...

+Job summary · Make a real difference in the lives of patients.+Monitor regulatory intelligence with stakeholders. · Prepare submission documents for Health Authorities. · ...

Astellas' Global Capability Centres – Overview Astellas' Global Capability Centres are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our thre ...

The Regulatory Affairs Group is responsible for ensuring that our products meet regulatory requirements and are approved for sale in various countries. The Senior Analyst will provide support to the C-ROSS(MS) Product Leader and Regulatory Regional Leader for regulatory activitie ...

We're looking for a detail-oriented Security & Compliance Analyst to own and manage customer security questionnaires, RFPs, and security reviews. · Own and complete customer security questionnaires... · ...

We're looking for a detail-oriented InfoSec Compliance Analyst to own and manage customer security questionnaires, RFPs, · and security reviews. Own and complete customer security questionnaires, · including SIG, CAIQ, VSA, · Maintain a centralized repository of up-to-date securi ...

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. · ...