Pre-clinical Research and Development jobs in Europe involving the drug discovery and design process. R&D jobs as a biochemist, geneticist, immunologist, medical chemist, microbiologist, molecular biologist, organic chemist, pharmacologist, scientist, toxicologist, including those in research institutes and universities. Find more pre-clinical research jobs on EuroScienceJobs.
Pre-clinical Research and Development jobs in Belgium (10), Croatia (1), Denmark (8), France (10), Germany (10), Hungary (1), Ireland (11), Italy (1), Multiple Countries (5), Netherlands (4), Romania (1), Switzerland (8) and United Kingdom (16).
Performing hands-on PBPK, QSP, and clinical trial simulations on an assigned project. Supporting the development of a team from both a technical and scientific perspective to ensure state-of-the-art mechanistic approaches are applied to optimize drug
Strategic and scientific leader within Clinical Development, driving the advancement of ProQR’s pipeline and contributing to improved patient outcomes. As a subject matter expert in CNS diseases, the Medical Director provides deep scientific and
Lead the scientific and operational design, conduct, implementation, and analysis of DMPK, ADME and PKPD studies to support the progression of discovery projects towards candidate selection and preclinical development using state-of-the art computational,
Leading our global investigative toxicology efforts with operations in Boston, Paris and Montpellier and with Senior Scientific Advisors serving as global safety experts in various toxicology disciplines based in multiple countries (France, US and
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development. Establishing and managing research projects as project scientist;
You will utilize your analytical chemical expertise to work at the intersection of chemistry and biology. Your focus will be on defining, developing, and optimizing analytical chemical methods, defining clinically relevant extractions for chemical
You will play a key role in advancing Lonza’s Vector Engineering R&D capabilities, leading innovative scientific projects and developing people, while contributing hands-on expertise in recombinant protein production and mammalian cell culture.
You will lead and execute advanced analytical strategies for biosimilar development. Your expertise ensures robust characterization of active pharmaceutical ingredients (API) and compliance with global regulatory standards. Design
Are you ready to lead cutting-edge analytical strategies for biologics? We’re looking for a Principal Analytical Scientist to drive method development, lifecycle management, and testing support for commercial products. This role is pivotal in
Manage a team of engineers, scientists and technicians in the development and implementation of new capsules, new capsules applications or related programs/projects in line with the R&D strategy and timelines; Define roadmap for the innovation
You will take on both strategic and operational responsibilities in advancing innovative therapies in autoimmune diseases, oncology, with a focus on advanced therapy medicinal products (ATMPs), including cell and gene therapies. In this role
You will play a key role in the design and development of immunohistochemical (IHC) assays and in situ hybridization (ISH) for in vitro diagnostics, working cross-functionally with scientists, laboratory technicians, production and external experts. You
Leads a team of Clinical Pharmacologist leads, providing strategic direction, leadership, and technical expertise for all aspects of clinical pharmacology studies across the IPSEN portfolio, including small molecules, peptides, and biologics (mAbs, ADCs,
You will perform extractables/leachables (EL) and elemental impurities (EI) assessments according to Lonza procedures and best scientific practices; Act as Lonza’s global EL/EI subject matter expert (SME) and ensure regulatory compliance of the global
In this lab-focused role requiring daily on-site presence, you will plan, execute and report on experiments that contribute to the discovery and characterization of new antibody-based therapies. You will work within a multidisciplinary project team and be
Development of the clinical pharmacology strategy of multiple programs spanning from candidate nomination for GLP toxicity studies through phase 4; Support clinical study protocol (phase 1-4) development, PKPD data analysis/interpretation, and study
Supervise Daily Laboratory operations, ensuring personnel execute their responsibilities in strict accordance with relevant regulatory guidelines. Support the weekly and daily production schedules and participate in the daily Tier 1 & 2 meeting
You are responsible for the development of the strategy and the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for investigational and commercial drugs to the sites of manufacture, both internal
Head a team specialising in the analysis of function and interaction for protein therapeutics. In this role, you will be responsible for driving the identification and commercialisation of innovative analytical methods and technologies that enhance the
The incumbent will perform the research, development, validation, and transfer of clinical laboratory tests into high-throughput routine operations for the diagnosis, treatment, and prevention of human disease. This role combines scientific innovation
Define and lead the scientific strategy for the therapeutic area, aligned with Evotec’s R&D and business objectives; Identify emerging opportunities based on scientific trends, competitive landscape, and unmet medical needs; Champion the therapeutic
You will provide scientific leadership for our liver programs, driving the discovery and development of novel RNA-based drug candidates for chronic liver diseases. You will shape scientific strategy, guide project teams in a matrix environment (without
The role of Laboratory Supervisor involves managing daily laboratory operations, ensuring the delivery of high-quality genomic analysis, and maintaining compliance with all regulatory standards. The successful candidate will play a key role in fostering a
Provide technical leadership for multiple PDS&T projects, including financial planning, budgeting, timeline estimation, and execution; Implement global projects across AbbVie plants and marketed affiliates, including oversight of products manufactured at
You will play a crucial role in driving the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials studying TransCon C-type natriuretic peptide (CNP). This is an exciting opportunity to work in a fast-paced environment,
Overseeing the overall end to end COE Research group covering pDNA, mRNA & Delivery (including Lipids discovery, associated synthesis) research teams and capabilities supporting Sanofi ambition in the field of therapeutic and prophylactic approaches
EuroScienceJobs is the best job board to find research and postdoc science jobs in Europe. Jobs in bioinformatics, biostatistics, biomedical research, biotechnology and genetics, microbiology and more. Research jobs across Europe including Belgium, France, Germany, Netherlands, Switzerland, UK and more.