We're sorry, the job you are looking for at EMA - European Medicines Agency on EuroPharmaJobs has expired.
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
The Associate Director Global Scientific Affairs Immunology, will be responsible for all aspects of scientific communications for the assigned asset, including strategy, planning...
The Senior Director Epidemiology leads epidemiology activities and/or projects in support of new drug development and/or post-marketing drug safety for the marketed products. The...
Establish and implement readouts for lysosomal (dys)function using biochemical and cellular assays as well as Omics techniques. Develop and supervise cellular assay systems based...
Independent authoring, editing and reviewing of various regulatory/clinical documents (e.g. aggregate reports, risk management plans and other documents needed throughout the...
As drug discovery expert, you combine a drug discovery industry background with scientific expertise in computational chemistry. You are a creative driver of change and experienced...
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...
Responsible for the scientific documentation concerning therapeutic areas/diseases, competitors, clinical standards/guidelines, medical and political environment. Assess study...
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...
As the Microbiology Technology Lead, you will act as a Subject Matter Expert (SME) for the global Ferring network, reporting to the CoE Analytics Director. In this role, you will...
The Global Medical Director Immunology and Inflammation - Nemolizumab is a subject matter expert in charge of providing the medical support to the development and execution of the...
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...
Plans and manages LSO timelines for assigned clinical trials, specifically the completion of the Lab Specifications and Kit Delivery. Participates in vendor meetings to ensure...
Statistical oversight of studies and assure adequate quality and consistency with project requirements; Responsible for the accuracy and completeness of database quality checks and...
As a Senior Scientist in the field of cell and molecular biology, you’ll play a vital role in the drug discovery processes based on structure-activity relationship studies or...
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...
Performing experiments/analyses and other enabling studies to support non-clinical studies, early phase, late phase; Supporting pre-formulation laboratory activities, which include...
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...
Achieve high levels of performance and engagement through inspirational and authentic leadership, coaching and mentoring of the Drug Product Operations team; Develop robust talent...
Study design, strategy, planning (timeline, required resources and budget) for QIAGEN sponsored clinical studies, coordinating activities with stakeholders internally and...
Lead formulation development activities related to liquid and lyophilized parenteral drug products of large molecule biologics (e.g. monoclonal antibodies, novel formats, ADCs,...
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...
Drive Quality Excellence to enable and improve process adherence, quality metrics, management review, and continuous improvement. Drive standardization and, where-ever it makes...
You will collaborate with project leaders to implement scientific technologies with minimal supervision to enhance productivity and efficiency within the Non-Clinical Safety...
Leads the development of the Global Medical Affairs strategy and execution of the Global Medical Affairs plan for select indications/projects related to evidence generation,...
For this vital role, we are seeking a skilled synthetic organic chemist to take part in an innovative Discovery Unit at Amgen Research Copenhagen with responsibilities including...
The Principal Statistical Programmer Analyst is accountable for the quality, timely, and efficient delivery of projects, programming work, and good information management. This...
You will be responsible for managing the Cell Biology team involved and ensuring the efficiency of the processes to meet the established milestones of projects. Your direct...
Be a point of contact of internal clients, especially Medical Affairs teams in terms of medical & scientific information; Conduct document searches based on internal clients’...
Provide scientific CMC input to the drug substance development strategy; Lead & participate in project teams, manage projects (scope, timelines, budget), and manage CDMOs on behalf...
As the medical senior manager, you will lead the Baltics Medical team, and you are an integral contributor in the Baltics management team as well as in cross-functional teams. You...
As our new Director of QA Commercial Drug Product & Finished Goods, you will be responsible to lead and support the team performing quality oversight and QP release of drug product...
As a Process Development Engineer, you will be responsible for development and improvement of manufacturing processes for biosurfactants as part of the lab and pilot team...
The Research and development director is part of the Leadership Team and responsible for developing long-term strategies for the R&D department and overseeing all aspects of...
For our laboratory processes and IVD medical device, your expertise is needed to further develop the risk-based approach for all processes and products that is triggered by an...
Implementation of the assigned international projects relating to the entire production network of the Group; Support and maintain the global Engineering and Maintenance framework...
Manage and lead a team of 4 LC-MS & MetID scientists; Ensure that robust LC-MS bioanalytical assays for small and large molecules are developed according to the sponsor and...
The person will have strong hands-on experience with mammalian cell culture (including some experience with hiPSC-derived cells), immunofluorescence/immunocytochemistry, standard...
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...
As a ProQR R&D Manager you will be key in leading a team (10-15 HC) of highly talented scientists and researchers in a matrix organization. You are a seasoned people leader with...
Provide leadership and scientific direction to the PR&D department; Ensure the provision of mentoring and development opportunities to facilitate progression opportunities for...
Define and implement the overall strategy for the manufacture of biological drug products through the various stages of development; Develop and structure the Drug Product (DP)...
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...
The role will provide scientific and technical leadership for analytical development at various stages of drug development including material characterization, analytical method...
Lead global CMC drug development projects from candidate profiling until successful regulatory approval and transfer to commercial manufacturing in a fully outsourced setting ...
Play a key scientific role in leading multiple drug discovery projects mainly in the area of neurosciences and with different modalities (small molecules, biologics, RNA targeting...
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...
In this role, you will be responsible for pharmaceutical manufacturing process validation. Leading the validation team for the process validation in the chemical plants. Ensuring...
Learning and implementing state-of-the-art innovative experimental and simulation techniques related to various unit operations; Developing prediction models based on various...
As a QC Team Leader you will take responsibility for the day-to-day operation of our QC Chemistry laboratory while also working with QC Management and fellow Team Leaders to devise...
We are looking for an enthusiastic, motivated and experienced Clinical and Retail Pharmacists. Permanent, part-time and contract positions available for pharmacists -...
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...
We’re looking for a Senior Project Manager to join our Cell and Gene Therapy Project Management team that is passionate about improving healthcare through innovative clinical...
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...
The I&TD Scientist specialist in organic synthesis, will play a central role within the team to design and execute experimental works in our labs and coordinate and lead relevant...
As the role holder, you will be responsible for ensuring the efficient management and control of the EMEA operation whilst achieving agreed budgetary and service levels. You will...
Manage registration related activities for LT and the other EU countries; Compile and submit applications for registration, renewals, variations in accordance to the national...
Provide Quality oversight of internal and external GxP operations, e.g. Drive, lead and troubleshoot quality investigations at internal and external partners to ensure that all...
As the Associate Director, Regulatory Affairs CMC you will be responsible and accountable for Regulatory CMC development, registration, and post-approval strategies. You will...
The Senior Manager of Commercial Supply Chain is responsible for supporting commercial third-party logistics (3PL) supply chain operations for Immunocore. Through strategic...