p style="margin:0in;font-size:12pt;font-family:'aptos' , sans-serif;line-height:115%">Qualifications: - Degree in scientific/life-sciences.
- Development of protocols for clinical studies.
Princeton, NJ30+ days ago p>As a Associate Scientist at Cyprotex, youll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. Cyprotex US specializes in ADME-Tox and Biosciences including both in vitro (laboratory experiments) and in silico (computer modelling) approaches. Wilmington, DE19 days ago Knowledge of modern data analytic tools, including machine learning, Design of Experiments, automated laboratory instruments (i.e. liquid/solid handling robot, autosampler), and analytical techniques (HPLC, GC, MS, NMR, UV-Vis, FT-IR, Raman and other PAT tools). Key Responsibilities: Independently propose, direct, and perform scientific experiments, including developing new flow chemistry methodologies, batch to flow conversions, and synthetic procedures in support of OLED material synthesis. Princeton, New Jersey30+ days ago A U.S. Department of Energy National Laboratory managed by Princeton University, the Princeton Plasma Physics Laboratory (PPPL) is tackling the world’s toughest science and technology challenges using plasma, the fourth state of matter. The University considers factors such as (but not limited to) scope and responsibilities of the position, candidate's qualifications, work experience, education/training, key skills, market, collective bargaining agreements as applicable, and organizational considerations when extending an offer. Princeton, New Jersey30+ days ago Expertise with handling of liquid metals, design and develop liquid metal experimental systems, liquid metal and and interpretation of material surface science diagnostics, and numerical simulations of liquid metal MHD is strongly preferred. The candidate will join a dynamic team of scientists with diverse expertise working to advance understanding and develop the science and technology of liquid metals to be used as plasma-facing components in fusion reactors. Collegeville, PA30+ days ago The role of Director, Global Real-World Evidence & Health Outcomes Research Scientist is critical to achieving this ambition by supporting asset teams to ensure that each medicine GSK brings to market is supported by scientifically credible, high quality, evidence that drives competitiveness and strong evidence-based product positioning, value propositions and value-based pricing. We need to better understand how our customers define value and to effectively collaborate with them to ensure we are generating value evidence data that includes real world evidence and cost effectiveness analyses that are impactful for payers, health systems, providers, and patients. p style="font-family:'calibri';font-size:10pt">The Real-World Evidence (RWE) team within Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group. This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Spring House, PA19 days ago p>Required Skills: Preferred Skills: Analytical Reasoning, Biological Sciences, Communication, Data Analysis, Data Compilation, Data Savvy, Design of Experiments (DOE), Drug Discovery Development, Execution Focus, Laboratory Experiments, Molecular Diagnostics, Pharmaceutical Microbiology, Product Knowledge, Project Management, Report Writing, Scientific Research, Technologically Savvy, Troubleshooting. Experience in cell culture, characterization of cell lines/tissue lysates by western blotting/qPCR/etc, cell proliferation assays including Incucyte-based assays, flow cytometry/FACS, CRISPR gene knockout and Lentiviral transduction of stable cell lines, cell imaging and other functional assays, etc. is needed. Spring House, PA1 day ago p>Required Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Biotechnology, Chemistry, Manufacturing, and Control (CMC), Clinical Research and Regulations, Clinical Trial Designs, Collaboration, Data Synthesis, Drug Discovery Development, Molecular Diagnostics, Pharmacovigilance, Process Improvements, Productivity Planning, Program Management, Scientific Research, Tactical Planning, Technical Credibility. Building trusted cross‑functional partnerships and influencing decision‑making across Therapeutics Discovery (TD), Preclinical Sciences & Translational Safety (PSTS), Therapeutic Areas (TAs), and TDS in matrixed governance and technical forums. North Wales, PA30+ days ago The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area. North Wales, PA12 days ago Assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility. Required Skills: Clinical Judgment, Clinical Medicine, Clinical Research, Clinical Trial Development, Clinical Trials, Data Analysis, Drug Development, Gastrointestinal Cancer, Gastrointestinal Oncology, Intellectual Curiosity, Mentorship. North Wales, PA30+ days ago Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology. North Wales, PA30+ days ago Required Skills: Clinical Development, Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Sciences, Clinical Trial Development, Clinical Trials, Drug Development, Intellectual Curiosity, Oncology, Oncology Research, Pharmaceutical Development, Strategic Planning. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area. North Wales, PA7 days ago li>Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. - Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs;
- Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and.
All Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America. Johnson & Johnson Innovative Medicine is recruiting for a Principal Data Product Scientist, DDSAI Immunology to join our Immunology R&D Data, Data Science & Artificial Intelligence (DDSAI) team and to enable and scale high‑value data assets across Immunology Research & Development. Spring House, PA30+ days ago Required Skills: Preferred Skills: Clinical Data Management, Critical Thinking, Drug Discovery Development, EHS Compliance, Emergency Planning, Organizing, Performance Measurement, Presentation Design, Process Hazard Analysis (PHA), Process Optimization, Program Management, Regulatory Affairs Management, Risk Management, Safety Audits, Safety Investigations, Safety-Oriented, Scientific Research. A minimum of 6 years of pharmaceutical/biotech industry experience in pre-clinical safety assessment supporting discovery/development with a Masters degree or a minimum of 3 years of pharmaceutical/biotech industry experience in pre-clinical safety assessment supporting discovery/development with a doctoral level degree (PhD, DVM, MD or equivalent) is required. p>Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus. West Point, PA17 days ago In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. The Senior Principal Scientist leads a team of health economists to develop and implement health economics and modeling strategies that enable the Company to understand and communicate the full economic value of the Company's oncology products to payers, health technology agencies, policy makers, and other decision-makers in order to optimize market access and patient outcomes. Support material qualification and requalification activities on behalf of the MSAT Material Science team: prepare qualification plans/protocols, coordinate testing with internal or external labs/vendors, analyze returned data, and draft qualification reports. The role will collaborate closely with Process, Planning, Manufacturing, Quality, Supply Chain/Procurement, Supplier Quality, and IT/data teams to improve raw material traceability, resolve material issues, and produce regulatory quality documentation. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. - Perform functionality testing on devices and support group scientists with device assembly and testing.
North Wales, PA22 days ago Under the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling. North Wales, PA29 days ago Required Skills: Biostatistics, Clinical Development, Clinical Outcomes, Collaborative Development, Communication, Data Management, Epidemiology, Health Economics, Health Technology Assessment (HTA), Market Access, Marketing Strategies, Neuroanatomy, Outcomes Research, Pathophysiology, Researching, Stakeholder Relationship Management, Strategic Planning. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, and systematic reviews and meta-analyses. North Wales, PA6 days ago ul>- Under the guidance of an Executive Director, the Principal Scientist/Director, has primary responsibility for developing value evidence strategies, and planning/managing real world and economic evidence activities for pipeline assets in rheumatology to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies and health systems globally.
- Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
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