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Independent authoring, editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports, risk management plans and other documents needed throughout the...
Serve as a scientific expert and point of contact for the oversight of Immunoassay development, validation, and clinical testing adhering to GCLP (Good Clinical Laboratory...
You will lead our global RA Team enabling us to drive forward with new and existing products within the global regulatory landscape. You will own and develop the strategies to...
The Director, Regulatory Sciences will formulate regulatory strategies and recommendations for the resolution of complex issues for clients and will lead the process in the...
The Senior Project Manager (Sr. PM) is responsible for the overall coordination and management of clinical trials from start up through to final delivery. This position directs the...
Manage and provide accountability for day-to-day operations of the project; Provide cross-functional oversight of internal project team members and deliverables, which includes...
Study design, strategy, planning (timeline, required resources and budget) for QIAGEN sponsored clinical studies, coordinating activities with stakeholders internally and...
Oversee the delivery of site management project tasks, providing advice and guidance to help achieve high performance and quality project deliverables; Develop, implement and...
You will provide strategic input into cross-functional drug development planning and execution across the product lifecycle, from discovery to postmarketing. You will ensure that...
To help us grow and lead our global PBPK/QSP business, we are looking for a Director/Lead Systems Pharmacology (m/f/d) to lead multi-disciplinary project teams through the...
In this role you are a true business partner offering valuable medical expertise in a compliant and ethical way; you contribute to the strategic objectives of Sanofi Vaccines by...
You will be responsible for running international/global studies in all therapeutic areas, managing the operational aspects of projects to meet contractual requirements. Using our...
Creating and maintain the clinical development plan and the clinical strategy for a research & development project in alignment with the target product profile to which you also...
A strategic and operational role, acting as part of the franchise brand team supporting development of strategy and tactical planning, ensuring the brand team have a deep...
As the Associate Director, Regulatory Affairs CMC you will be responsible and accountable for Regulatory CMC development, registration, and post-approval strategies. You will...