38 Jobs für Clinical Drug Scientist
Stellenangebote Clinical Drug Scientist Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
[. .. ] 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 [...]
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[...] strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead 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 [. .. ] 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 [. .. ]
Job gestern 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 id: [...]
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[...] 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 [. .. ]
Job gestern bei Jobleads gefunden
• 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 [...]
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[...] 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) [. .. ] IB 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. 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 [. .. ]
Job gestern bei Jobleads gefunden
Principal Scientist, Toxicology
• Opfikon, Zürich Zuerich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead 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 non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role : The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities : [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
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 [...]
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[...] 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 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist (m/f/d) (LSW) - BS
• Binningen, Basel- Landschaft
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 [...]
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[...] 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 [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Berlin
Principal
Scientist (m/f/d) - Oncology Location: Berlin We are looking for a Principal Scientist to join the newly established Ni V (Novel in vitro Phenomics) team. This role is ideal [...]
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[...] for someone passionate about developing innovative in vitro models and using them for drug development and discovery projects that drive meaningful impact for patients. Ni V is part of the Oncology Translational Research (OTR) team at GSK and is embedded in a collaborative network across OTR and beyond, supporting both preclinical and clinical development programs within the GSK Oncology Therapeutic Area. The successful candidate will join a team currently being built across Berlin and Stevenage, with a core focus on establishing cuttingedge organoid models and leveraging them across a range of translational applications, from chemosensitivity profiling to molecular engineering approaches for biomarker discovery [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist (6754)
• Dallenwil, Basel, Nidwalden, Basel- Stadt
Medical Device
Clinical Safety
Scientist 6754 Our client is a leading Swiss multinational healthcare company headquartered in Basel, Switzerland. Operating in Pharmaceuticals and Diagnostics, it is one of the [...]
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[...] worlds largest biotech companies and a global leader in in-vitro diagnostics and cancer treatments. Our client is known for its strong focus on innovation, particularly [. .. ] 3 years relevant Healthcare, Scientific or biomedical research background in clinical safety with the use of MDs and/or combination products in the pharmaceutical/ biotech or MD industry Background in drug safety (pharmacovigilance) is an additional asset Strong understanding of the biomedical technical aspects of MDs. Working knowledge of relevant MD regulations and industry standards. MD clinical investigations expertise: significant expertise and handson experience in safety activities related to (Class II and/or III) MD clinical investigations, evidenced by practical experience [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Medical Device Clinical Safety Scientist
• Basel, Basel- Stadt
Medical Device
Clinical Safety
Scientist 6754 Our client is a leading Swiss multinational healthcare company headquartered in Basel, Switzerland. Operating in Pharmaceuticals and Diagnostics, it is one of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the worlds largest biotech companies and a global leader in in-vitro diagnostics and cancer treatments. Our client is known for its strong focus on innovation, particularly [. .. ] 3 years relevant Healthcare, Scientific or biomedical research background in clinical safety with the use of MDs and/or combination products in the pharmaceutical/ biotech or MD industry Background in drug safety (pharmacovigilance) is an additional asset Strong understanding of the biomedical technical aspects of MDs. Working knowledge of relevant MD regulations and industry standards. MD clinical investigations expertise : significant expertise and handson experience in safety activities related to (Class II and/or III) MD clinical investigations, evidenced by practical [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• 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 [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead 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 [. .. ] 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 [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Toxicology
• Zürich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead 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 non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities:Serve as the [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Zürich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead 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 non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities:Serve as the [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
• 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. [...]
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[...] 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 [. .. ]
Job am 09.11.2025 bei Jobleads gefunden
Scientist Drug Product Development AH
• Ingelheim am Rhein, Rheinland- Pfalz
The Position We are looking for a dynamic and experienced professional to take on the role as
Scientist Drug Product Development AH in our esteemed pharmaceutical company. In this position, [...]
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[...] you will have the opportunity to showcase your experiences in the context of cuttingedge pharmaceutical development of drug products. With a strong focus on solid and semisolid preparations, you will play a pivotal role in shaping the future of [. .. ] you to apply for this exciting opportunity. Tasks responsibilities You will take responsibility for the development of innovative NCE drug products, guiding them from early formulations to final processes, including clinical trial material manufacturing and packaging development activities. As a key member of our team, you will represent Pharmaceutical Development (PD) in crossfunctional project teams. In your role, you will work according to predefined Quality Target Product Profiles (QTPP) and global regulatory requirements. You will organize our lab units by taking [. .. ]
Job am 19.10.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Dortmund, Nordrhein- Westfalen
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 [. .. ]
Job am 10.10.2025 bei Jobleads gefunden
Analytical Scientist
• Basel, Basel- Stadt
[. .. ] within the Interiman Group, we offer tailor-made solutions in personnel consulting. For our client F. Hoffmann-La Roche in Basel, we are looking for a motivated and reliable [...]
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[...] Analytical Scientist 80-100. Responsibilities Developing a phase-appropriate control strategy for pharmaceutical dosage forms, encompassing the active ingredient and its precursors. Collaborating effectively with stakeholders across various departments, including drug substance and drug product process development and manufacturing, Technical Regulatory Affairs, Quality Assurance, and both internal and external analytical partners (such as service providers and commercial manufacturing/ testing/ packaging sites) . Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/ improving and validating analytical test [. .. ] charged aerosol detection A comprehensive understanding of quality control principles is essential. Demonstrated experience in applying Good Manufacturing Practice (GMP) requirements and a clear understanding of their application across different clinical phases. Digital acumen to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageous. Excellent command of the English language. Proficiency in German is considered a plus. Superior communication skills and a proven ability to collaborate successfully. Open-minded, goal-oriented, and capable of thriving in [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] Lead, RLT Senior Project Manager IT and Digitalisation Technical Project Manager HVAC, Cleanroom, EMS, ALC Manager Global Business Excellence--Temporary position Muttenz, Basel-Country, Switzerland 1 year ago Global [...]
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[...] Drug Regulatory Affairs Project Leader (6602) Associate Director, Technical Project Leader Drug Substance Senior Project Manager: Public Infrastructure Finance for Municipal Development Permanent contract Analytical Project Leader Senior/ Principal Scientist Lead, Real World Sciences Application Strategy m/f/d Drug Product Project Leader Oral Dosage Forms (80-100) Consultant Technology Transfer-Fill Finish Team Lead MES PI Competence Center (f/m/d) , 80-100 Senior Global Business Process Specialist Financial Accounting Senior Clinical Operations Manager-6575 Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 65375776 [. .. ]
Job am 05.10.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Essen, Nordrhein- Westfalen
Overview 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 cross-functional team involved with [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
Junior Research/ Technology/ Clinician-Scientist Group Leaders (m/f/d)
• Hannover, Braunschweig, Niedersachsen
Führungs-/ Leitungspositionen Absolventen, Einsteiger, Trainees
Human Microbe Alliance for Universal Health (HUMAN) program The Helmholtz Centre for Infection Research (HZI) , is offering positions for Junior Research/ Technology/ Clinician-
Scientist Group Leaders (m/f/d) in the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field of infection research with W1-professorship and tenure options) HZI is Germanys largest academic institution dedicated to infection research. It is a member of the Helmholtz Association, Germanys largest research organization, and a member of the German Center for Infection Research (DZIF) [. .. ] processes of human tissues and microbial entities. To use microbial effector and resilience mechanisms shaped by millions of years of microbial evolution as blueprint for engineering human and planetary health. Clinical research with a focus on infection biology to tackle patient-oriented questions and pioneer solutions for human infection resilience and health of tomorrow. Research and technology areas of particular interest include, but are not limited to, microbiology, phages, virology, immunology, vaccinology, AI and systems biology, spatial OMICS, drug research, digital epidemiology, precision infection medicine, RNA-biology, human tissue engineering, One Health research, or synthetic viral and bacterial engineering. Hypothesis-driven, clinical and foundational research as well as the development of breakthrough technologies are welcome to enable interdisciplinary and transformative scientific discoveries. Requirements : You are a highly qualified [. .. ]
Job am 22.09.2025 bei Jobleads gefunden
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Planegg, München, Bayern
Clinical Scientist-Manager/ Senior Manager (m/f/d) Permanent employee, Full-time Planegg (Germany) , Remote (Germany) Be part of our team As a Clinical Scientist (m/f/d) and member of our Clinical Development team, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 cross-functional team involved with [. .. ]
Job am 07.09.2025 bei Jobleads gefunden
Medical Director/ Exec. Director, Gastrointestinal (GI) Immunology (Translational Medicine)
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] success of early global programs, develop and implement strategies to achieve Transition Decision Point (TDP) . Drive success of late global programs by developing and implementing strategies, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] which lead to clinical pharmacology and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling. Support Translational Research in developing new indications, endpoints and biomarkers, using in vitro, in vivo, or in silico methods. Provide scientific expert assessments and support for in-licensing opportunities, including due diligences. Major Accountabilities Early Clinical Projects (Phase I/ II, Discovery) Develop, in collaboration with TM TA Head and [. .. ] and written) . About Translational Medicine Translational Medicine is a global group of scientists and physicians working at the pre-clinical and early clinical stage of drug discovery. Our Physician-Scientist Discovery Profiling group drives innovative science from Discovery to the market and focuses on early clinical drug development with cross-functional collaboration to bridge preclinical research and clinical development, tailoring to patient needs and personalized medicine. Diversity, Inclusion, and Accessibility Novartis is committed to diversity and inclusion and to providing [. .. ]
Job am 23.08.2025 bei Jobleads gefunden
Director Bioinformatics (m/f/d)
• Hamburg
Führungs-/ Leitungspositionen
Jobticket
[. .. ] oncology. For almost 25 years, we have been driven by a single, overarching vision: a world in which precision therapy offers a cure for every cancer patient. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Specialized in early drug discovery, our R D approach is based on the belief that we need to fundamentally understand the disease to gain novel insights and develop effective therapeutics. To do so, we start with carefully collected and curated patient samples, resulting in a comprehensive and proprietary database. By employing advanced biomathematical and [. .. ] our shared purpose, we explore the complexity of cancer with curiosity and determination. Thriving on innovation, we value unique perspectives and visionary scientific approaches to grow together. Whether as a scientist, as a data analyst, or in a corporate function everyone contributes to our common goal. If you thrive on discovery, come join our team and make your impact We are looking for a Director Bioinformatics (mf/d) Your responsibilities As Director of Bioinformatics you will become the driving force behind [. .. ] industry best practices in software validation and data security. Develop and apply advanced statistical and AI methods to model biological systems and predict therapeutic outcomes. Work with LIMS, IT, and clinical data science teams to integrate bioinformatics workflows into clinical and research pipelines. Support key partnerships with networking clinics, academic institutions, and pharmaceutical collaborators to drive bioinformatics innovation in oncology. Stay abreast of the latest developments in bioinformatics, biomathematics, and related fields, and apply innovative approaches to enhance our R D [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
Bayer
Senior Scientist (all genders) - in Vitro CVRI
• Berlin
[. .. ] join 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 [...]
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[...] one choice. Senior Scientist (all genders) - in Vitro CVRI Join Bayers Cardiovascular, Renal and Inflammation (CVRI) research area and contribute to pioneering therapies for kidney diseases. In this laboratory-focused role, you will design and execute cutting-edge 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 hands-on expertise within one of our technology areas [. .. ]
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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 38 offene Stellenanzeigen für Clinical Drug Scientist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Drug Scientist Jobs?
Aktuell suchen 6 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 (10 Jobs)
- Bayer (1 Job)
- Fraunhofer- Gesellschaft (1 Job)
- GSK (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 (13 Jobs), Nordrhein-Westfalen (6 Jobs) und Berlin (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Scientist Jobs?
Clinical Drug Scientist Jobs gehören zum Berufsfeld Pharmazie.
