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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

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

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.

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.

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 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.

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

Associate Principal Scientist, Post Market Safety, L'Oréal Research & Innovation - Clark, New Jersey. At L'Oréal Research & Innovation we are pushing the boundaries of Science & Tech. We invest heavily in cutting-edge research, leveraging advanced technologies to understand skin, hair, and microbi

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

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.

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.

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

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

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.

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

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

Duration: 03 Months assignment (possibility of extension).Location: Plainsboro, NJ 08536.QC Temporary Technician primary responsibilities are to complete testing and final Quality disposition decision on Quality Control Samples received through the use of approved SOP's.Manage the receipt of samples

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 al

Job Title: Data Governance & Process Mapping Consultant (W2 Contract – Onsite).Location: Matawan, NJ ( On-Site 5 days).US citizens and Green Card Holders and those authorized to work in the US are encouraged to apply.We are unable to sponsor H1b candidates at this time.Data Governance, Data Qu

Application should include a CV, cover letter, Research Statement describing your previous research contributions, specific role in those projects, and future research goals, including how your expertise and interests align with the focus of The Guzman-Velez Lab at Rutgers University. William Hu, ai

The Postdoctoral Research Assistant will lead impactful research studies, develop their own research questions, publish in scientific journals, and continue their own scholarly and research development. Ability to work well independently and in a collaborative team environment including research ana

The R&D Lab Technician is a detail-oriented quality focused individual who will support the Food Scientists within the R&D Department at New Classic Cooking. This role will work to assist the scientists as well as organize the lab ingredients to set the team up for success. Support new product testi

The initial appointment will be for two years at Rutgers University followed by a third year appointment held at CCA as a Flatiron Research Fellow. The successful applicant will contribute to a research program on star formation, galaxy formation, the interstellar medium and fluid dynamics. Postdoct

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

Disseminate research findings (analyzing data, writing manuscripts, presenting at conferences);. Seek external funding for projects (both supporting PI grant submissions, as well as establishing funding for their independent line of research);. Postdoctoral Research Associate.

Director, Research & Development. 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.

This includes oversight of the Office of Human Research Services, the clinical Disease Specific Groups, clinical research related shared resources, and inter-programmatic meetings with clinical and translational researchers across the Cancer Institute. Our renowned faculty are teachers, health resea

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

Senior Scientist/Principal Scientist, Quantitative Pharmacology (Contractor). Strong independent scientific research ability, logical thinking, and coordination/problem-solving skills.

We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the wo

Senior Food Scientist, Cheese Product Development. Our client is seeking a passionate and innovative Senior Food Scientist - Cheese Formulator to join their Global Dairy and Alternative Dairy Applications team. Strong ability to translate scientific research into commercially viable manufacturing ap

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 are seeking a skilled Project Manager to join our team in Warren, NJ.Under the general supervision of the Branch Manager, perform daily management and oversight of the current projects, including but not limited to project management, business development, financial management, staff development,