Clinical Drug Scientist Stellenangebote


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Stellenangebote Clinical Drug Scientist Jobs


Job vor 5 Tagen bei StepStone gefunden Miltenyi Biotec B. V. Co. KG

Senior Clinical Scientist Clinical Drug Development (m f d)

• Bergisch Gladbach Homeoffice möglich Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers, using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market As a Senior Clinical Scientist in Clinical Drug Development, 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 contribute to the development and execution of global clinical development plans (Phases IIII) [. .. ]

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Job gestern bei Jobleads gefunden Senior Principal Scientist (all genders) • Berlin Senior Principal Scientist (all genders) Senior Principal Scientist (all genders) Arbeitsort Berlin Beginn Biologe/ Biologin At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] world where, Health for all, Hunger for none is no longer a dream, but a real possibility. Were doing it with energy, curiosity [. .. ] a community of brilliant and diverse minds to make a real difference, theres only one choice. Senior Principal Scientist (all genders) YOUR TASKS AND RESPONSIBILITIES You are responsible for leading drug discovery programs, initiatives, or collaborations in Research/ Early Development (RED) Oncology from target identification up through support of early clinical development You support and contribute to the drug development strategy of RED Oncology and the matrixed management and coaching of peers and other colleagues in RED Oncology to support multiple drug development programs You support the career development and scientific strategic coaching of colleagues in Research Oncology You collaborate with [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden

Principal Scientist as Biomarker Lead for Neuroscience and Mental Health

• Biberach an der Riß, Baden- Württemberg Führungs-/ Leitungspositionen Principal Scientist as Biomarker Lead for Neuroscience and Mental Health Were looking for a motivated Principal Scientist to help shape the future of clinical development in the field of neurodegeneration, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] psychiatry, and mental health. As a Principal Scientist, you will play a key role in driving innovative translational strategies across the entire clinical development pipeline, with the ultimate goal of being firsttopatients. In this strategic position, you will support the clinical drug research and development process by strategic planning and execution of data generation, all aspects of data analytics, and by developing and implementing translational strategies with a specific focus on biomarkers in human patient populations. This position can be filled in Ingelheim or Biberach. It is parttime eligible with 80 effort. [. .. ]

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Job vor 2 Tagen bei Jobleads gefunden Field Application Scientist, Europe • Hamburg [. .. ] Tru Cytes cell mimics precisely replicate real cells optical and biochemical properties-without the sourcing, quality, or cost challenges of traditional controls. Trusted in cell-based applications across cell [...]
MEHR INFOS ZUM STELLENANGEBOT[...] therapy, drug development, and diagnostics, they empower process and analytical development, quality control, potency assessments, multi-site validations, clinical research studies, and assay development and validation. Slingshot is seeking motivated, creative team members who think outside the box. We empower employees to own their work, contribute ideas quickly, and improve processes. Come join our cross-disciplinary and world-class team that is delivering game-changing solutions for cell-based [. .. ] Participate in industry conferences, trade shows, and customer site visits to represent Slingshot Biosciences and build relationships within the scientific community. Qualifications 3+ years of experience in a field application scientist role or related technical support position, preferably within the life sciences or biotechnology industry. Required: Bachelors in a relevant scientific discipline (e. g. , Biology, Biochemistry, Biotechnology, Biomedical Engineering) or equivalent experience. Masters or Ph. D. is desirable in a relevant scientific discipline or equivalent experience. Strong understanding of synthetic [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

Senior Principal Scientist (all genders)

[. .. ] us. If youre hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, theres only one [...]
MEHR INFOS ZUM STELLENANGEBOT[...] choice. Senior Principal Scientist (all genders) YOUR TASKS AND RESPONSIBILITIES You are responsible for leading multiple drug discovery programs, initiatives, or collaborations in Research/ Early Development (RED) Oncology from target identification up through support of early clinical development You support and contribute to the drug development strategy of RED Oncology and the matrixed management and coaching of peers and other colleagues in RED Oncology to support multiple drug development programs You support the career development and scientific strategic coaching of colleagues in Research Oncology You collaborate with [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Senior Data Scientist II-Therapeutic Modality Insights Competitor Intelligence (all genders) • Ludwigshafen am Rhein, Rheinland- Pfalz [. .. ] your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place Together, we break through [...]
MEHR INFOS ZUM STELLENANGEBOT[...] as Senior Data Scientist II Therapeutic Modality Insights Competitor Intelligence (all genders) Abb Vies global Information Research (IR) group has a mission to unlock information that makes cures possible. Within IR, the Enterprise Knowledge Accelerator (EKA) team is the trusted knowledge partner for clients in R D and the Corporate Business Strategy Office (CBSO) [. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation [. .. ] data pipelines and analytical workflows for large and complex published (often unstructured) data, including literature publications, patents, news/ press releases, and competitor pipelines. Demonstrate deep knowledge of pharmaceutical R D, drug development, and therapeutic modality trends Operate with high autonomy and productivity, proactively tackling complex problems and driving multiple projects with minimal supervision. Pursue and evaluate relevant external and internal leads in novel modalities, new technologies, and data sourcesrapidly incorporating new findings into project strategies and generate novel, actionable insights for [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

Postdoc Biomedical Data Scientist

• Sankt Augustin, Nordrhein- Westfalen [. .. ] in industrial practice as partners to industry. The Biomedical AI Data Science team is dedicated to the development and application of cuttingedge data science approaches (specifically machine [...]
MEHR INFOS ZUM STELLENANGEBOT[...] learning) in early drug discovery, precision medicine and clinical trials. The team is internationally well connected and is working closely together with leading European and US institutions from academia and industry in multiple research projects. What you will do Development application of innovative algorithms in the field of machine learning, specifically with focus on decision support in medicine and [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden Scientific Engagement Manager • München, Bayern [. .. ] teams (ranging from bench scientists to Heads of R D) to diagnose their specific therapeutic challenges. Design and guide proofofconcept studies that demonstrate the clear utility of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] our models in drug discovery and translational research. Adoption Expansion : Proactively identify opportunities to expand the scope of the partnership. Leverage your understanding of the clients pipeline to suggest new use cases, therapeutic areas, or departments where our technology can drive value. Product Intelligence Roadmap Influence Voice of the Customer : Synthesize technical [. .. ] Educational Background : Ph D in Computational Biology, Bioinformatics, Genomics, or a related field is required. Domain Expertise : Deep understanding of the biopharma R D value chain (target discovery to clinical trials) . You understand the specific pain points of drug developers. Technical Fluency : Extensive experience with multiomics datasets (singlecell, transcriptomics, proteomics) . You can comfortably discuss ML concepts (LLMs, benchmarking) with data scientists. Relationship Strategic Skills Stakeholder Management : Proven experience navigating complex, matrixed organizations (Big Pharma experience is [. .. ] with a bioinformatician in the afternoon. Consultative Mindset : You are not just a support agent; you are a trusted advisor. You have experience in roles such as Field Application Scientist (FAS) , Solution Architecture, or Scientific Consulting. Feedback Synthesis : Ability to distill complex client complaints or requests into clear, prioritized product requirements. How to stand out Experience in a startup or innovative environment, showing adaptability and proactiveness. A strong existing network within Global Top 20 Pharma R D. Experience [. .. ]

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Job vor 3 Tagen bei Jobleads gefunden

Senior CMC Scientist

• Berlin We are seeking a Senior CMC Scientist (Biologics) to support late-stage development and lifecycle management of biologic drug products (e. g. monoclonal antibodies, recombinant proteins, or advanced biologics) [...]
MEHR INFOS ZUM STELLENANGEBOT[...] . This role will play a key part in CMC strategy, regulatory submissions, and technical oversight for EU and global programs. Berlin-based biotech companies typically value handson expertise combined with regulatory awareness, and this role reflects that balance. Key Responsibilities CMC Development Lead and support CMC development activities for biologic drug substances and drug products Act as a CMC subjectmatter expert for one or more clinical or commercial biologics Contribute to control strategy development (CQAs, CPPs, specifications) Support process characterization, comparability, and change control Oversee analytical method development, qualification, and validation for biologics Review and interpret stability, release, and characterization data Regulatory Documentation Author, review, and maintain CMC sections of regulatory dossiers : IMPD (EU) CTA [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden NLP Data Scientist/ Scientific Data Engineer x2 • Heidelberg, Baden- Württemberg [. .. ] EBI provides world-leading chemogenomics resources to the scientific community including Ch EMBL, a database of quantitative small-molecule bioactivity data curated primarily from the scientific literature widely used [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to support drug discovery projects in industry and academia. The Safety 2.0 project is funded by Open Targets, a unique public-private partnership working to deliver experimental data and informatics resources that enable scientists to make more informed decisions about target selection for developing safer and more effective drugs. You will interact [. .. ] the Chemical Biology Services and Open Targets groups, benefitting from a range of multi-disciplinary expertise and technologies. Develop machine learning pipelines for extracting drug side effects from drug labels, clinical trials, publications and other documents Investigate modern NLP methodologies and propose ideas for the implementation of data extraction methods and pipelines Apply language models to extract and map drug-related information from unstructured text, e. g. from the scientific literature, Clinical Trials. gov Implement and/or fine-tune different NLP [. .. ]

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Job vor 5 Tagen bei Jobleads gefunden

Senior Data Scientist II Therapeutic Modality Insights Competitor Intelligence (all genders)

• Ludwigshafen am Rhein, Rheinland- Pfalz Work-Life-Balance Senior Data Scientist II Therapeutic Modality Insights Competitor Intelligence (all genders) 1 day ago Be among the first 25 applicants Unternehmensbeschreibung Abb Vies mission is to discover and deliver [...]
MEHR INFOS ZUM STELLENANGEBOT[...] innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact [. .. ] knowledge and insights mining and analysis, as well as designing and building innovative selfservice solutions for insights generation from published resources and internal knowledge. This includes literature, patent, conference, news, clinical trial, and competitive intelligence data such as competitor pipelines. As a Senior Data Scientist on the Solutions for Published Insights Client Enablement (SPICE) team, you will serve as the lead data scientist focused on advancing Abb Vies competitiveness by driving Therapeutic Modality Knowledge Intelligence Solutions. You will lead the creation [. .. ] data pipelines and analytical workflows for large and complex published (often unstructured) data, including literature publications, patents, news/ press releases, and competitor pipelines. Demonstrate deep knowledge of pharmaceutical R D, drug development, and therapeutic modality trends. Operate with high autonomy and productivity, proactively tackling complex problems and driving multiple projects with minimal supervision. Pursue and evaluate relevant external and internal leads in novel modalities, new technologies, and data sourcesrapidly incorporating new findings into project strategies and generate novel, actionable insights for [. .. ]

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Job vor 7 Tagen bei Jobleads gefunden Junior/ Senior/ Principal Scientist-Systems Pharma/ Toxicology (PBPK-QSP/ T) • Niedersachsen Absolventen, Einsteiger, Trainees Homeoffice möglich Are you a talented and motivated life-science modelling simulation scientist with experience in the pharma industry? Do you enjoy driving innovation and setting new boundaries in physiologically-based (PBPK) modelling, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] pharmacokinetics, quantitative systems pharmacology and toxicology (QSP/ T) ? This position offers you this and more exciting work in an innovative and fast-paced environment. ES Qlabs is an innovative, [. .. ] multi-disciplinary project teams for the successful completion of client goals. Role Complement a dedicated high-performing team of scientists Collaborate with colleagues on multi-disciplinary teams to implement quantitative clinical pharmacology projects/ programs and to provide clinical pharmacology and PBPK/ QSP consultation to other company projects/ programs Provide clinical pharmacology and pharmacometric consulting through advanced QSP and exposure-response modeling and simulation using the OSP-Suite (PK-Sim, Mo Bi, R) , or other tools Support clinical pharmacology-related components [. .. ] prepare abstracts, presentations, and publication-ready manuscripts Provide mentoring and feedback to junior scientists Integrate knowledge of PBPK, PK/ PD, and QSP to provide guidance regarding proposed approaches to addressing drug development and regulatory approval challenges Expand scientific expertise through attendance and presentation at international, national, and regional scientific conferences, client meetings, and government meetings Develop and teach at OSP-Suite (PK-Sim, Mo Bi, R) , and other workshops and courses Required skills experience 3+ (Senior: 6+, Principal: 10+) years [. .. ]

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Job vor 8 Tagen bei Jobleads gefunden

Lead Clinical Scientist Drug Development (m f d)

• Bergisch Gladbach, Nordrhein- Westfalen Führungs-/ Leitungspositionen Lead Clinical Scientist Drug Development (m f d) Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious lifethreatening [...]
MEHR INFOS ZUM STELLENANGEBOT[...] diseases and reshaping accessibility worldwide. We focus on difficulttotreat hematological cancers using CART and other technologies, and we explore treatments for other diseases. Our [. .. ]

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Job am 09.12.2025 bei Jobleads gefunden Scientist (m/f/d) for the area LC/ MS (full-time) • Frankfurt, Hesse Scientist (m/f/d) for the area LC/ MS (full-time) Apply for the Scientist (m/f/d) for the area LC/ MS (full-time) at Kymos Group. Sector: Pharmaceutical and biopharmaceutical Location: Frankfurt am [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Main, Germany Contract: Permanent Working day: Full time Vacancies: 1 Discipline: R D Work modality: On [. .. ] committed to promoting diversity, gender equality, wellbeing, and initiative, encouraging career development and internal promotion. Job Description As an LCMS Scientist, you will generate highquality bioanalytical data supporting our clients drug development programs. You will develop and validate LCMS/ MS methods according to ICH M10 guidelines, perform study sample analysis under GLP, and work on projects ranging from preclinical studies to Phase IIII clinical trials and bioequivalence studies. Your Key Responsibilities Develop, optimize, and validate LCMS/ MS methods for small molecules and/or biomolecules in biological matrices. Plan and perform sample preparation, instrumental analysis, data processing, and data evaluation. Execute study sample analysis in compliance with GLP and internal SOPs. Document experimental work and [. .. ]

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Job am 08.12.2025 bei Jobleads gefunden

Senior Data Scientist-Literature (m/f/d) (LSW) - BS

• Basel, Basel- Stadt Homeoffice möglich [. .. ] For 75 years, weve operated in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects. We are looking for [...]
MEHR INFOS ZUM STELLENANGEBOT[...] a Senior Data Scientist-Literature m/f/d LSW-BS Background The position of Senior Data Scientist Literature sits within the Safety Analytics and Reporting SAR group of the Safety Risk Management PDS function. In this role, you support Roches product portfolio by conducting global literature searches and extracting information from biomedical databases to [. .. ] as Periodic Safety Update Reports PBRERs. As many of these deliverables are mandated by health authorities, the role requires consistent quality, adherence to timelines, and close alignment with stakeholders from Clinical Science, Safety Operations, PDMA, Regulatory Affairs and related functions. The insights generated from these analyses form a crucial component of patient-focused risk assessment. You will further contribute by supporting projects, improving processes, and participating in strategic initiatives that strengthen Roches safety strategy. The Ideal Candidate The preferred candidate holds a university degree in medicine, pharmacy or life sciences and brings at least two years of experience in Information Science, ideally with strong exposure to pharmacovigilance and drug development. We are looking for a proactive, analytical and collaborative individual with excellent communication skills and the ability to train others. Strong organisational skills, a continuous improvement mindset and the ability to build effective cross-functional relationships are essential for success in this role. General Information Start date: asap Latest [. .. ]

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Job am 08.12.2025 bei Jobleads gefunden Principal Scientist, Toxicology • Zürich Principal Scientist, Toxicology CSL CSLs R D organization is accelerating innovation to deliver greater impact for patients. With a projectled structure and a focus on collaboration, were building a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] futureready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary: Project Toxicology Role: The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, leads the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of nonclinical safety studies conducted internally [. .. ] Development representative in Research Project teams. Design, oversee, and interpret nonclinical safety studies (GLP and non GLP) to support regulatory submissions and drug development. Develop and implement toxicology strategies aligned with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk [. .. ]

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Job am 07.12.2025 bei Jobleads gefunden

Senior Clinical Development Lead-Early Trials

• Morges, Waadt A leading biotechnology company in Switzerland seeks a Sr. Director Clinical Research Scientist to provide clinical research support across various programs. This role entails developing protocols for clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] studies, leading clinical teams, and ensuring compliance with regulations. The ideal candidate possesses strong analytical skills, excellent communication abilities, and preferably prior experience in oncology drug development. The position offers a dynamic work environment and values diverse experiences. #J-18808-Ljbffr 71923068 [. .. ]

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Job am 07.12.2025 bei Jobleads gefunden Senior Scientist (all genders) - in Vitro CVRI • Berlin Senior Scientist (all genders) - in Vitro CVRI At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a world where Health for all, Hunger [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for none is no longer a dream, but a real possibility. Were doing it with energy, curiosity and sheer dedication, always learning from [. .. ] diseases. In this laboratory-focused role, you will design and execute cuttingedge in vitro experiments, drive innovation in molecular and cellular analytics, and play a key role in advancing our drug discovery programs from target validation to clinical evaluation. Your Tasks And Responsibilities You will design and execute in vitro experiments (cellular, enzymatic, biochemical) , analyze data, and present results and next steps in the context of kidney disease modelling to advance CVRI drug discovery programs You will provide handson expertise within one of our technology areas (Biochemistry [. .. ]

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Job am 07.12.2025 bei Jobleads gefunden

HTE Principal Associate/ Scientist in Process Chemistry Catalysis (2 year fixed term contract)

• Basel, Basel- Stadt [. .. ] and for generations to come. Join Roche, where every voice matters. The Position The Process Chemistry Catalysis (PTDC-C) team is dedicated to designing and developing robust and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] cost-effective drug substance processes using state-of-the-art science and methodologies. Our critical work supports the synthetic molecules portfolio from the initial entry into human trials through the transfer to commercial manufacturing, including the necessary support for regulatory submissions. We are a key part of Small Molecules Technical Development (PTDC) , which develops our synthetic pipeline and manufactures drug substance and drug product for clinical studies, collaborating closely with research partners and the commercial manufacturing network. We are seeking a highly motivated and technically skilled early career scientist to join the PTDC-C team. This is a handson laboratory role situated at the nexus of modern chemistry, automation, and data science, where you will be a key driver in our stateoftheart High Throughput Experimentation (HTE) laboratory. This position directly impacts our clinical pipeline by accelerating the discovery and [. .. ]

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Job am 05.12.2025 bei Jobleads gefunden HTE Principal Associate/ Scientist in Process Chemistry Catalysis • Basel, Basel- Stadt HTE Principal Associate/ Scientist in Process Chemistry Catalysis page is loaded # # HTE Principal Associate/ Scientist in Process Chemistry Catalysislocations: Baseltime type: Full timeposted on: Posted Todayjob requisition [...]
MEHR INFOS ZUM STELLENANGEBOT[...] id: 202511-129598At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and [. .. ] where every voice matters. # # # # # The Position The Process Chemistry Catalysis (PTDC-C) team is dedicated to designing and developing robust and cost-effective drug substance processes using state-of-the-art science and methodologies. Our critical work supports the synthetic molecules portfolio from the initial entry into human trials through the transfer to commercial manufacturing, including the necessary support for regulatory submissions. We are a key part of Small Molecules Technical Development (PTDC) , which develops our synthetic pipeline and manufactures drug substance and drug product for clinical studies, collaborating closely with research partners and the commercial manufacturing network. We are seeking a highly motivated and technically skilled early career scientist to join the PTDC-C team. This is a hands-on laboratory role situated at the nexus of modern chemistry, automation, and data science, where you will [. .. ]

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Job am 30.11.2025 bei Jobleads gefunden Clinical Scientist-Manager/ Senior Manager (m/f/d) Clinical Scientist-Manager/ Senior Manager (m/f/d) Direct message the job poster from Tubulis Gmb H Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical Development [...]
MEHR INFOS ZUM STELLENANGEBOT[...] team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and crossfunctional team involved with site [. .. ]

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Job am 27.11.2025 bei Jobleads gefunden Clinical Scientist-Manager/ Senior Manager (m/f/d) • Leipzig, Sachsen Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our [...]
MEHR INFOS ZUM STELLENANGEBOT[...] antibody-drug conjugates (ADCs) global clinical trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and cross-functional team involved with [. .. ]

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Job am 26.11.2025 bei Jobleads gefunden Principal Scientist (all genders) - in Vitro CVRI • Berlin Principal Scientist (all genders) - in Vitro CVRI At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a world where, Health for all, Hunger [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for none is no longer a dream, but a real possibility. Were doing it with energy, curiosity and sheer dedication, always learning from [. .. ] Bayers Cardiovascular, Renal and Inflammation (CVRI) research area and play a key leadership role in advancing our kidney disease portfolio. You will lead in vitro pharmacology initiatives from concept to clinical translation, drive scientific innovation, and guide cross-functional teams to develop transformative therapies for patients worldwide. Your Tasks And Responsibilities You will drive the development of a sustainable renal disease research portfolio within Bayers CVRI organization You will hold full accountability for in vitro pharmacology across project teams, providing strategic guidance and acting as Biology Lead where required You will design, supervise, and innovate functional in vitro disease models (cellular, enzymatic, biochemical) to advance renal disease drug discovery You will take a leading role in technology teams, promoting agile resource management and driving technical innovation You will proactively engage in Disease Biology Communities and initiate novel target proposals to expand the CVRI portfolio You will coach and mentor scientists and technical staff, fostering excellence, collaboration, and innovation [. .. ]

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Job am 22.11.2025 bei Jobleads gefunden Medical Device Clinical Safety Scientist (m/f/d) (LSW) - BS • Basel, Basel- Stadt Homeoffice möglich [. .. ] needs. For 75 years, weve operated in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects. We are looking [...]
MEHR INFOS ZUM STELLENANGEBOT[...] for a Medical Device Clinical Safety Scientist m/f/d LSW-BS Overview/Background The Portfolio Clinical Safety PCS organisation provides scientific safety expertise and vigilance support for medical devices and molecules across the entire Roche portfolio. The team oversees all safety-related responsibilities, with accountability shared between PCS leadership and specialised Safety Strategy Leaders SSLs, depending [. .. ] and RSI, including the ability to independently lead the development of these deliverables. Strong background in benefit-risk assessment and medical device risk management aligned with ISO 14971. Experience with drug/ device combination products. Excellent communication, leadership and teamwork skills. Nice to Have Background in drug safety pharmacovigilance Dissatisfied, unchallenged, or eager to discover something new What are you waiting for Apply now, unlock your potential, and aim for greater satisfaction in your career. Im here to support you with my [. .. ]

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Job am 11.11.2025 bei Jobleads gefunden Principal Scientist, Regulatory Toxicology • Glattbrugg, Zürich Principal Scientist, Regulatory Toxicology Join to apply for the Principal Scientist, Regulatory Toxicology role at CSL. CSLs R D organization is accelerating innovation to deliver greater impact for patients. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] With a projectled structure and a focus on collaboration, were building a futureready team that thrives in dynamic biotech ecosystems. Joining CSL now [. .. ] part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. The role serves as the primary toxicology representative on interdisciplinary project teams, leads the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. Responsibilities include design, budgeting, and monitoring of nonclinical safety studies in GLP and non GLP environments. The role [. .. ] Development representative in research project teams. Design, oversee, and interpret nonclinical safety studies (GLP and non GLP) to support regulatory submissions and drug development. Develop and implement toxicology strategies aligned with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Clinical Drug Scientist pro Jahr?

Als Clinical Drug Scientist verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Drug Scientist Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 50 offene Stellenanzeigen für Clinical Drug Scientist Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Scientist Jobs?

Aktuell suchen 8 Unternehmen nach Bewerbern für Clinical Drug Scientist Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Drug Scientist Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Drug Scientist Stellenangebote:


  • Tubulis GmbH (11 Jobs)
  • Abb Vie (2 Jobs)
  • Bayer (2 Jobs)
  • Miltenyi Biotec B. V. Co. KG (1 Job)
  • Fraunhofer- Gesellschaft (1 Job)
  • Sanofi (1 Job)


In welchen Bundesländern werden die meisten Clinical Drug Scientist Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Drug Scientist Jobs werden derzeit in Niedersachsen (17 Jobs), Nordrhein-Westfalen (10 Jobs) und Berlin (7 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Drug Scientist Jobs?

Clinical Drug Scientist Jobs gehören zum Berufsfeld Pharmazie.


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