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This role designs and executes elaborate experiments for pharmaceutical sciences projects and demonstrates resourcefulness in running multiple activities concurrently, all related...
Lead formulation development activities related to liquid and lyophilized parenteral drug products of large molecule biologics (e.g. monoclonal antibodies, novel formats, ADCs...
The clinician medical monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for...
Ensure customer service level promises and logistics costs with the cluster VP & EMEA SC VP. In accordance with the Cluster Executive Committee, lead the Cluster Order Policy...
Responsible for Neuropsychiatry products launch activities, cross-functional leadership and management of Medical Science Liaisons (MSLs). You will represent medical affairs at...
Interpret data to develop strategies and lead complex scientific projects considering EU/UK regulatory requirements; Efficiently and effectively manage multiple projects so...
You will lead the clinical development strategy and be responsible for designing and executing clinical development plans for MR Imaging assigned contrast agents...
Provides leadership in multiple therapeutic areas including pipeline products across a broader geographical scope. He/she reports directly to the Senior Medical Director CE...
You will lead scientific studies while independently analyzing and interpreting data and proposing next steps. You design, lead development, and act as subject matter experts of...
You will provide therapeutic and drug development expertise and interact with Sponsors and investigative sites on protocol medical issues. Contribute to investigator meeting...
We are looking for a multidisciplinary scientist to drive end-to-end scientific operations, from product development to quality control. Ideal candidate will excel in scientific...
The candidate will contribute, with internal and external partners, to project proposals and innovative approaches in the field of antibody/biologics discovery to deliver high...
In line with defined product responsibilities, utilize regulatory expertise to develop and deliver optimal regulatory strategies and plans to support the achievement of country...
Develop and implement quality transformation strategies: You will be responsible for designing and implementing strategies to improve quality standards across the organization....
The CTM Team Leader will be overseeing and preforming of manufacturing (cell- and tissue culturing) of cell therapy products in accordance with GMP regulations. As well as being...
The Director Assay Development leads an international and multidisciplinary team of scientists and lab technicians who have their main focus on developing a completely new...
The successful candidate will be responsible for the in vitro cellular pharmacology function within the drug discovery team. You will use your extensive experience in people...
Develops, deploys and delivers OTC strategy aligned with global, Europe and International Market strategy; Defines focus and prioritize for investment in alignment with regions and...
We are looking for a Bioanalyst to provide “hands-on” bespoke bioanalytical services, including developing and undertaking analyses for small molecules and peptides, across a...
The Head of Quality UK & Ireland will be responsible for the direct supervision of the company concerning all activities covered by the MHRA Establishment license and HPRA rules....
As the Director Protein and Cell Supply you will be responsible for the supply chain from vector design to protein production to logistics. You will lead three processes (and...
This high-level scientific position requires extensive experience in the area of analytical separation and characterization of biotherapeutic proteins, with key focus on protein...
Manages audit planning, assignments, support, and reporting of research and development submissions, pre-clinical, Clinical Research (GCP), Pharmacovigilance (PV), Laboratory (GLP)...
Rhythm is looking for a Sr Manager QA to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical and...
Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated...
This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally. The role...
The candidate with be responsible for creating and maintaining Medical Affairs slide decks. The Medical Writer will collaborate with Medical Affairs stakeholders to create...
You will be responsible for leading global, complex extractables and leachables (E&L) projects with internal and external laboratories. You will work with site and global teams to...
Lead Global Med. Excellence and Stakeholder Engagement Team (Med. Communication, Med. Info, Capabilities and Learnings, Medical Service Hub, Medical Evidence Generation Management...
Your key responsibilities will be people management, coordinating screening workflows for projects at different discovery stages, and maintaining a versatile assay platform...
Create and Review regulatory documentation for Drug, Device and Combination product renewals with major focus on Medical Device renewals; Track status and progress of regulatory...
This position is responsible for the study-level management (prior to submitting to IRB/EC to closeout) of clinical studies, including preparation of applicable clinical study...
Develop and maintain excellent thought leader relationships in the field of rare disease specifically Fabry Disease, Pompe Disease and Batten Disease; Lead on medical initiatives...
Responsible for managing GCP and GVP Quality Management Systems of Research and Development activities in accordance with applicable legal, regulatory and other Quality standard...
Moderna is seeking a talented, experienced, and motivated Senior Scientist to join the Immuno-Assays group to serve as a scientific expert and point of contact for the oversight of...
As an (Associate) Director, Global Regulatory Affairs Project Lead you will join our Global Regulatory Affairs organization. In this capacity, you will assume responsibility for...
Play a key scientific role in multiple projects in the field of preclinical/clinical biomarkers in (immuno)oncology by participating in cross-functional biomarkers projects....
Derives targets from a thorough assessment starting with biology and a deep understanding of genetics. Shapes the identification and prioritization of disease areas for the...
Director, Clinical Research Scientist is responsible for working with the physicians within Clinical to provide clinical research support for programs as assigned by phase or...
The External Manufacturing Manager plays a pivotal role in overseeing and managing all aspects of drug product manufacturing operations. This role requires a strategic leader with...
As Manager, DMPK and PK/PD Modeling, you will lead our Drug Metabolism and Pharmacokinetics (DMPK) activities. In this role you will have the opportunity to develop scientific...
Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices to enhance the value of our oncology pharmaceutical...