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Adherence to all Good Manufacturing Practices (GMP) Safety Standards.Join Us as an Associate Research Scientist Make an Impact at the Forefront of Innovation.We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countr

It is university policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression

This role is ideal for someone with a strong foundation in.Master's Degree in AI, Machine Learning, Computer Vision, or a related field.Minimum 5 years of professional experience in medical imaging, AI, machine learning, or deep learning.Experience in Deep Reinforcement Learning (DRL).Proficient in

As a Research Scientist within Global Analytical Sciences, you will provide critical analytical support to Product Development, Early Research teams, and global manufacturing sites.

Rutgers, the State University of New Jersey has opening for Research Scientist II at the Rutgers Institute for Nicotine and Tobacco Studies located in New Brunswick, NJ. The Research Scientist II is responsible for research studies, including design, analysis, and reporting.

Join our dynamic team as a Principal AI/ML Research Scientist, where you will play a pivotal role in advancing cutting-edge artificial intelligence technologies.

Scientist/QC Sample Management.

Colgate-Palmolive is seeking a highly motivated and proactive Senior Research Scientist/Principal Scientist in the Research & Innovation Oral Care Group, Global R&D.

A minimum of $402,703 for assistant professor. This is a tenure track position at the Assistant or Associate Professor level that requires excellence in clinical practice and demonstrated accomplishments in scientific research. Radiation Oncology Physician Scientist; Tenure Track (Assistant to Assoc

Job Title: Post-Graduate/Post-Doctoral Research Scientist, Sterile Product Development. We are seeking a highly motivated post-graduate student or postdoctoral level scientist to join the Sterile Product Development organization at Client's New Brunswick, NJ site.

Job Description Company Overview: We are a dynamic and innovative small biotechnology company dedicated to advancing oncology research through cutting-edge translational science. Our mission is to translate scientific discoveries into tangible therapeutic solutions that make a meaningful impact on cancer patients' lives. We are seeking a talented and motivated Translational Scientist to join our team and contribute to our mission-driven work. Position Overview: As a manager of clinical pharmacology you will be responsible for providing clinical pharmacology input in early (up to proof-of-concept stage) and late-stage clinical development. You will be responsible for representing clinical pharmacology function on drug development teams, providing input on the dose and the design of early and late-stage clinical trials, and for interacting with the clinicians and the clinical operations group for the execution of the clinical pharmacology components (PK, PD, biomarkers, etc) of the trials. In addition, you will be responsible for performing clinical PK/PD analyses, for providing subject matter leadership related to clinical ADME, pre-clinical to clinical extrapolation and selection of dose/regimen during early development. Additionally, you will be responsible for providing input on study design and leading the selection of doses for late-stage clinical studies. You will contribute to the preparation of the regulatory documents such as briefing books for pre-agency meetings, IBs, INDs, and IMPD dossiers, protocols, and clinical study reports. You will closely collaborate with other development-functions (Toxicology, Bioanalytical, Non-clinical PK/PD, Pharmacometrics and Physiological PK/PD Modeling and Simulation, Biomarkers, Biostatistics and Data Management, Clinical Operations, and Clinical Development) to bring drug candidates from IND stage to NDA. You will be responsible for working within the department level budget and resources. Support technical due diligence efforts for business development. Responsibilities: • Responsible for providing support for the preparation of the clinical pharmacology (PK, biomarkers, bioanalytical) sections of early and late-stage clinical protocols, Clin Pharm development plans, modeling & simulation plans, • Contribute to the preparation of the pre-IND, IND, IB and NDA/BLA documents, • Responsible for the pharmacokinetic and PK/PD data analyses using standard industry data analysis software, • Contribute to the design of early phase clinical trials (FIH to POC) and support project goals, • Responsible for recommending the starting dose in FIH trials based on allometric scaling or physiologically based PK modeling, • Conduct assessments of relevant exposure vs. response data for supporting dose selection during and post POC, • Contribute to the design of late-stage clinical trials (POC-NDA/BLA) and support project goals, • Responsible for leading the dose selection for Phase II and III clinical trials based on PK, PD biomarker and efficacy data analysis from previous studies., • Responsible for the preparation of the PK/PD reports and clinical study reports, • Represent Clin Pharm function for the project team at the regulatory agencies during regulatory meetings., • Provide clinical pharmacology input and collaborate across all areas of drug development, along with research, preclinical, bioanalytical and clinical development functions., • Provide oversight to vendors and ensure high quality deliverables that meet study/project timelines, • 3+ years of pertinent post-doctoral experience in supporting pharmacokinetics, pharmacodynamics and other clinical pharmacology components of early clinical trials within the pharmaceutical or biotech industry., • Exposure to biologics drug development. Knowledge of basic and clinical immunology is plus., • Hands on knowledge of PK/PD and statistical analyses methods used in analyzing early clinical phase data., • Knowledge of general regulatory process and experience in contributing to IND, EOP1, EOP2, and pre-BLA/NDA meetings with the FDA , EMA and other health authorities., • Excellent written and oral communication skills including good presentation skills. Qualifications: • Doctoral degree (PhD or Equivalent training by experience) in clinical pharmacology, pharmacokinetics, pharmacology, or relevant life science discipline such as biology, immunology., • Hands-on experience with pharmacokinetic/pharmacodynamic data analyses using standard industry data analysis software., • Familiar with PK/PD concepts. principles and applications to support prospective dose/regimen recommendations for planned Phase 1, 2 and 3 trials., • Experience in preparing clinical pharmacology components of clinical study protocols and clinical study reports., • Knowledge of current practices and issues in the bioanalytical and drug metabolism areas., • Proficient in the use of Microsoft Word, Excel and PowerPoint. Travel: • Ability to travel domestic and internationally ≤ 20%. Benefits: Competitive salary commensurate with experience Comprehensive benefits package, including medical, dental, and vision coverage Opportunities for career growth and professional development Collaborative and dynamic work environment with a diverse team of scientists and clinicians Opportunity to make a meaningful impact on cancer patients' lives through innovative translational research

Job DescriptionSalary: Princeton NuEnergy (PNE) is excited to announce future opportunities to join our innovative Research & Development team, focused on pioneering advancements in the direct recycling and upcycling of spent Lithium-ion battery materials. Our mission is to deliver a cost-efficient, environmentally friendly solution to the current industry pain points of high operational costs and low efficiency in battery recycling. We aim to solve these challenges by improving battery recycling efficiency and purity, thereby revolutionizing the lithium-ion battery recycling landscape. About Us: PNE is a lithium-ion battery direct recycling and critical materials recovery innovator, founded out of Princeton University. At its core, PNE's patented recycling technology is based on a low-temperature plasma-assisted separation process (LPAS) that does not damage but, rather, reclaims and repairs cathode material from spent lithium-ion batteries and manufacturing scrap at half the cost with significantly lower waste when compared with existing traditional recycling processes. Our state-of-the-art laboratory is located in Princeton, New Jersey, where we are dedicated to pushing the boundaries of sustainable energy technologies. We are building a team of passionate and talented individuals to drive forward our cutting-edge research initiatives. Potential Roles: We anticipate openings for the following positions in the near future: • Research Scientist, • Process Engineer We welcome applications from candidates with expertise in: • Battery cathode material synthesis and related research experience., • Plasma physics, particularly in device development and experimental applications., • Chemical Engineering (with a focus on inorganic chemistry), Materials Science & Engineering, Chemistry, or related areas of study. If you are passionate about sustainability, innovation, and advancing the future of energy storage, we would love to hear from you! Princeton NuEnergy, Inc. is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, gender, sexual orientation, gender identity or expression, religion, national origin, marital status, age, disability, veteran status, genetic information, or any other protected status under federal, state, and local laws.

Job Title: Post-Graduate/Post-Doctoral Research Scientist, Sterile Product Development. We are seeking a highly motivated post-graduate student or postdoctoral level scientist to join the Sterile Product Development organization at Client's New Brunswick, NJ site.

Associate Principal Scientist, Post Market Safety, L'Oréal Research & Innovation - Clark, New Jersey. As an Associate Principal Scientist in Post Market Safety, your responsibilities will include:. At L'Oréal Research & Innovation we are pushing the boundaries of Science & Tech.

One of our large MedTech clients is looking for a Clinical Research Scientist to join their team for a 12+ month project.

Clinical Director (Principal Scientist). Participation in internal and joint internal/external research project teams relevant to the development of new compounds. Supervise the activities of Clinical Scientists in the execution of clinical studies.

Senior Clinical Research Scientist. The Clinical Research Scientist (CS) in Clinical Development is an important role in the company supporting the development and life cycle of drug development projects. The Clinical Research Scientist will work closely with the Clinical Trial Lead/Medical Lead and

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. Facilitate collaborations with external researchers around the world. Minimum of 1 year of industry e

Principal Scientist, Medical Device Expert, Research & Innovation, Safety Evaluation, Regulatory Affairs and Claims Substantiation & Microbiology (SRCM) - Clark, New Jersey (Hybrid). We are seeking a Principal Scientist, Medical Device Expert to join our Safety Evaluation, Regulatory Affairs and Cla

Whether your background is in data science, astrophysics, economics, biostatistics, operations research, or any other quantitative field, if you think rigorously about data and models, your skills are directly applicable here.

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies. Most research studies are conducted remotely at home, though some may be in-person.

Medical Affairs Project Manager.Raritan, NJ (3 days onsite per week).Contract Medical Project Manager.Cardiovascular product medical launch.The ideal candidate brings strong.Medical Affairs launch readiness.Medical Affairs, Global & regional partners, Alliance partners and cross functional colle

Our RMS business in Moorestown, NJ is a hub of talented engineers, scientists, and professionals committed to shaping the future of defense technology.

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies. Most research studies are conducted remotely from home, though some may be in-person. Comfort participating in remote, market r

DataAnnotation is committed to creating high-quality AI.Join our team to help train the next generation of AI while enjoying the flexibility of remote work and the freedom to set your own schedule.This role is designed to fit a variety of lifestyles — whether you're looking to contribute part-t

Excellent communication and stakeholder management skills to interact with researchers, lab managers, and vendors.

Sciens Building Solutions seeks an experienced Project Manager (PM) responsible for the execution of fire and life safety system projects in accordance with project budgets, code compliance, and managing the field operations team's work quality and work output.This position will work closely with ou

DataAnnotation is committed to creating high-quality AI.Join our team to help train the nextgeneration of AI while enjoying the flexibility of remote work and the freedom to set your ownschedule.This role is designed to fit a variety of lifestyles — whether you’re looking tocontribute part-time

We will prioritize the recruitment of candidates who demonstrate research excellence in areas of clinical science that complement and/or expand the current research foci of our department, especially candidates who have expertise in smartphone-based real-time monitoring and the analytic techniques r

Candidates with a strong background in transportation infrastructure and experience in research project management are preferred. The candidate is expected to advance research in transportation infrastructure durability, resilience, safety, facilitate interaction with various stakeholders, and organ

We have an opening for a temporary.Clark, NJ 07066 Note: online applications accepted only.Monday - Friday, hours may vary.Previous experience is preferred, but not required.ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the Intern

Assist in the development and optimization of formulations for various dosage forms such as tablets, capsules, and granules, under the direction of senior formulation scientists or supervisors. Director, Research & Development.

Our renowned faculty are teachers, health researchers and providers, and scientists with unparalleled experience who advance medical innovation and provide patient care informed by the latest research findings. This includes oversight of the Office of Human Research Services, the clinical Disease Sp

We have an opening for a temporary.Note: online applications accepted.Monday - Friday, hours may vary.Previous experience is preferred, but not required.ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the International WELL Building

The post-doctoral position will also provide opportunities to contribute to a variety of additional research projects at VTC in collaboration with faculty and research staff. Post-Doctoral Research Associate. Voorhees Transportation Center (VTC ) of the Bloustein School of Planning and Public Policy

Our client is a wellestablished construction management and development firm recognized for delivering highquality commercial interior projects throughout New Jersey and the surrounding region.With a commitment to professionalism, transparency, and strong relationships, the organization prides itsel

Postdoctoral Associate - Astrophysics (Rutgers-CCA Flatiron Research Fellow). The Rutgers University Department of Physics and Astronomy invites applications for a postdoctoral research position starting on, or after, 7/01/2026. The successful applicant will work at the galaxy-interstellar medium in

Job Title: Communications Project Manager.This contractor role supports with Promotional Material Review (PMR) operations and Veeva Vault PromoMats, supporting the end-to-end promotional material review (PMR) process.This position supports the Director of Content Excellence to ensure the promotional

Insight Global is looking for a Project Manager to help support one of our large pharmaceutical clients, specifically to support their CAR-T Manufacturing organization.The goal of this candidate will be FMEA, risk and gap assessment for end to end processes related to manufacturing their final thera