St. Luke's Health Network, Inc.Clinical Research Coordinator I- Precision Medicine St. Luke's Health Network, Inc.Clinical Research Coordinator I- Precision MedicineAllentown, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
Daiichi Sankyo, Inc.Sr Clinical Study Assoc CO Daiichi Sankyo, Inc.Sr Clinical Study Assoc COBasking Ridge, NJ$100,960–$151,440 / yearFull timeKey focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Job Description. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.
Daiichi Sankyo, Inc.NewManager, Clinical Adjudication Operations Daiichi Sankyo, Inc.Manager, Clinical Adjudication OperationsBasking Ridge, NJ$127,280–$190,920 / yearFull timeBecome a Subject Matter Expert (SME) with the process currently in use; be able to describe to study teams and other key departments how their study will interact with the adjudication vendor; Describe the expectation and importance of adjudication between the vendor to the CRO; Become an active “extended team member” to multiple studies at the same time; Being extremely organized to discuss with studies at different timepoints. Support analysis of study site ILD adjudication metrics reports to identify potential areas of concern, trends, missing eDC pages, issues with image uploading; bring to the attention of the Study Team / CRO; offer solutions.
YANTRAN LLCResearch & Development, Scientist 2 YANTRAN LLCResearch & Development, Scientist 2Summit, NJ$30–$35 / yearFull timeWork closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP).
Theradex OncologyClinical Research Associate (CRA) – All levels (I/II/Senior) Theradex OncologyClinical Research Associate (CRA) – All levels (I/II/Senior)Princeton, New JerseyWe will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate’s qualifications, experience, skills, and competencies for the role. As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.
IQVIA Holdings IncClinical Research Associate, Full Service IQVIA Holdings IncClinical Research Associate, Full ServiceParsippany, NJ$47,400–$169,300 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigators Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Atlantic Health System IncClinical Research Associate, Full Time Days 8a-4p, Atlantic Health, Morristown Medical Center Atlantic Health System IncClinical Research Associate, Full Time Days 8a-4p, Atlantic Health, Morristown Medical CenterMorristown, NJAtlantic Health scored four A grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. Morristown Medical Center is a Magnet Hospital for Excellence in Nursing Service, the highest level of recognition achievable from the American Nurses Credentialing Center for facilities that provide acute care services.
SystimmuneSenior Clinical Research Associate SystimmuneSenior Clinical Research AssociatePrinceton, NJFull timePrepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
Actalent IncNewClinical Research Nurse Coordinator Actalent IncClinical Research Nurse CoordinatorNew Brunswick, NJ$55–$60 / hourThis position assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and provides protocol-related clinical management to participants while on study. The position is part of a large clinical operations team with disease-specific groups, contributing to high enrollment needs across multiple sites, including Newark and other locations.
St. Luke's Health Network, Inc.Clinical Research Coordinator II- Precision Medicine St. Luke's Health Network, Inc.Clinical Research Coordinator II- Precision MedicineAllentown, PAFull timeThis includes performing required study procedures as applicableApply knowledge and skills to independently review new protocols, consents, and other clinical trials documents to ensure protocol complianceReview and extract data from medical charts to screen patients for eligibility for assigned protocolsReview consent form, protocol procedures, and treatment regimen with potential patients and obtain consent from interested participants, documenting the consent process as requiredMaintenance of accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subjects logs and study-related communicationOrganizational management of all aspects of the trial including but not limited to timeliness in completing case report forms (CRFs), data entry, reporting adverse drug events, managing caseload and managing study filesObtain data from other departments (radiology, pathology, etc.) as required by each protocolPrepare research charts for monitoring visits and auditsRespond to data queries and collate data as requested by research group or investigator, and maintain quality source documentation PHYSICIAL AND SENSORY REQUIREMENTS: Requires sitting for up to seven hours per day, 4 hours at a time. Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.
System OneSenior Clinical Research Associate System OneSenior Clinical Research AssociatePlainsboro Township, New Jersey$115,000–$130,000 / yearTrain and support external trial staff regarding CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability, temperature monitoring, query resolution, essential document collection, and ITF filing. Collaborate with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues impacting trial milestones.
Rutgers The State University of New JerseyTemporary Research Assistant Rutgers The State University of New JerseyTemporary Research AssistantNew Brunswick, NJ$35–$45 / hourSpecial Conditions Posting Details Posting Number 25ST0473 Posting Open Date Special Instructions to Applicants Regional Campus Rutgers Biomedical and Health Sciences RBHS Home Location Campus Downtown New Brunswick City New Brunswick State NJ Location Details Pre-employment Screenings All offers of employment are contingent upon successful completion of all pre-employment screenings. Aligned with Rutgers University-New Brunswick and collaborating university-wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and research, neuroscience, advanced biotechnology, and medicine, environmental and occupational health, and health care policy, and aging research.
ETSSenior Research Assistant ETSSenior Research AssistantPrinceton, NJ$64,000–$74,000 / yearThrough strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere.
Ferring Pharmaceuticals, Inc.Director, Clinical Research Alliances Ferring Pharmaceuticals, Inc.Director, Clinical Research AlliancesParsippany, NJ$178,000–$210,000 / yearResponsibilities: Contribute to and support the company’s efforts in communicating the high value of Ferring Uro-oncology research initiatives to successfully execute trial needs Initiate and maintain relationships with study investigators to create advocates for Ferring Uro-Oncology research Collaborate with the Therapeutic area medical team and medical affairs to support current PI involvement and KOL engagement initiatives Uncover opportunities for engagement to ensure appropriate enrollment at each research center Collaborate with Ferring clinical operations, TA medical directors, and CRO to identify and develop key performance indicators (KPIs) for activities aimed at enhancing trial recruitment, and ensure reports are developed and shared with management to track progress and drive improvements Work with Ferring clinical operations, TA Medical Directors and CRO to understand KPIs for enrollment and support where necessary for optimal study performance – then delete this as incorporated in above Work to facilitate collaboration between different departments or groups within the same study site to optimize the enrollment of trial participants, feeding back any trial-specific impact to the Ferring clinical operations team to ensure coordinated efforts Report identified site or vendor issues to Clinical trial team via TA medical directors including opinions and observations related to the operational, scientific and other aspects of the study so that Ferring clinical operations team can assess appropriate trial-related actions Collaborate with Ferring medical affairs and CTT during the start-up phase for selection of sites to enable and retain beneficial experiences and best practices Ensure alignment of medical communications and publications plans within the overall medical brand and development plan – delete as this has too much overlap with existing teams and processes Support and partner with key internal business partner Ensure effective interaction & communication between the uro-oncology research team, medical science liaison teams and other key stakeholders Requirements: Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 15+ years in matrix leadership organizations in operational or client facing environments. Experience working with Urologist preferred Prior medical affairs, medical communications, publications and/or KOL management experience highly desired Proven leadership track record with exceptional communication, collaboration and prioritizing skills, supporting pre and post-launch activities.
ETSResearch Associate ETSResearch AssociatePrinceton, NJThe Research Associate provides independent technical support to research projects with minimal guidance from senior staff, supports the coordination and execution of the scope of work of research projects, participates in coordinating staff efforts across multiple roles (e.g., research assistants, scientists, data analysts, engineers, program administrators, directors, etc.), and contributes as a co-author to presentations or publications. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide.
Judge GroupAssociate Director Clinical Research & Development Judge GroupAssociate Director Clinical Research & DevelopmentParsippany-Troy Hills, NJ$150,000–$175,000 / yearBy providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Identify gaps in pre-clinical and Phase 1 DDP that could impact Phase 2/3 design and execution timelines for company internal projects as well as programs being evaluated as part of due diligence.
SanofiClinical Research Director SanofiClinical Research DirectorMorristown, NJ$178,500–$257,833.33 / yearReporting to the Global Project Head, the CRD leads clinical trial strategy of assigned program(s) within the clinical development team, including interactions with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Colgate-Palmolive CompanyNewSr. Director, Clinical Research (Piscataway, NJ, US) Colgate-Palmolive CompanySr. Director, Clinical Research (Piscataway, NJ, US)Piscataway, NJ$250,000–$275,000 / yearDevelop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.
VitaliefOncology Clinical Research Nurse Director VitaliefOncology Clinical Research Nurse DirectorNew Brunswick, NJFull timeIMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. Vitalief partners with Sponsors, CROs, and research sites across the clinical trials ecosystem, delivering consulting and workforce solutions that improve efficiency, reduce costs, and accelerate patient-impacting innovation.
VitaliefSenior Clinical Research Coordinator VitaliefSenior Clinical Research CoordinatorNew Brunswick, NJFull timeResponsibilities:Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol-specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Phase 1 Oncology trials. IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP.
VitaliefClinical Research Change Management Consultant VitaliefClinical Research Change Management ConsultantNew Brunswick, NJRemotePart timeThe ideal candidate brings deep expertise in organizational transformation and change management within complex healthcare and research environments, with a proven ability to drive stakeholder alignment, operational adoption, and sustainable process improvement across multi-site systems. Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs.
VitaliefOncology Nurse (RN) – Clinical Research Career Opportunity VitaliefOncology Nurse (RN) – Clinical Research Career OpportunityNew Brunswick, NJFull timeIMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.
VitaliefOncology RN – Clinical Research Nurse (Training Provided) VitaliefOncology RN – Clinical Research Nurse (Training Provided)New Brunswick, NJFull timeIMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.
VitaliefClinical Research Strategic Management Consultant VitaliefClinical Research Strategic Management ConsultantNew Brunswick, NJRemotePart timeThis role will serve as the primary subject matter expert (SME) for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness. Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations.
RD PartnersAssociate Research Scientist RD PartnersAssociate Research ScientistLawrenceville, New Jersey£65,977–£82,472Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.
Atlantic Health SystemLead Clinical Research Nurse, Part Time Days, 8a - 4p, Atlantic Health, Morristown Medical Center Atlantic Health SystemLead Clinical Research Nurse, Part Time Days, 8a - 4p, Atlantic Health, Morristown Medical CenterMorristown, NJAtlantic Health scored four “A” grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. In addition, Leapfrog recognized us with an \"A\" hospital safety grade - its highest - twelve consecutive times, and the Centers for Medicare and Medicaid Services awarded us again with its highest five-start rating in 2020.
VitaliefVice President, Clinical Research FSP Consulting VitaliefVice President, Clinical Research FSP ConsultingNew Brunswick, NJRemoteFull timeProven success in building strong executive-level and C-suite relationships while leading a multi-faceted change process; demonstrated broad-based change management expertise and extensive experience positively influencing change in a variety of complex environments with multiple stakeholders and competing priorities. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .
SystimmuneClinical Research Associate II SystimmuneClinical Research Associate IIPrinceton, NJFull timePrepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
VitaliefClinical Research Coordinator VitaliefClinical Research CoordinatorNew Brunswick, NJFull timeIMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .
Rutgers The State University of New JerseyNewBioinformatics - Assistant to Associate Professor, Non-Tenure Research Track Rutgers The State University of New JerseyBioinformatics - Assistant to Associate Professor, Non-Tenure Research TrackNew Brunswick, NJTo accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities. Experience and peer-reviewed publications in which the incumbent has performed the tasks listed below are strongly preferred: Spatial transcriptomics: Analysis and integration of spatially resolved gene expression data to characterize tissue architecture, cell-cell interactions, and microenvironmental heterogeneity.
VitaliefClinical Research Coordinator (CRC) – Infectious Disease VitaliefClinical Research Coordinator (CRC) – Infectious DiseaseSomerset, NJFull timeIMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .
Sunrise Systems IncAssociate Research Scientist Sunrise Systems IncAssociate Research ScientistLawrenceville, NJ$37–$39 / hourThe qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists. The ideal candidate would be able to work independently, demonstrate flexibility, and a willingness to work as a member of a large cross-functional team.
Lehigh UniversityPostdoctoral Research Associate in Industrial and Systems Engineering Lehigh UniversityPostdoctoral Research Associate in Industrial and Systems EngineeringBethlehem, PAThe Department of Industrial and Systems Engineering in the Rossin College of Engineering and Applied Science at Lehigh University seeks a motivated and talented Postdoctoral Research Associate to contribute to our research initiatives and academic programs. This role offers a unique opportunity to work with Professor Andrew Goldberg in the field of industrial and systems engineering, engage in cutting-edge research, and gain experience in mentorship and academic service.
Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLCInternational Medical Graduate (IMG) - Clinical Research CoordinatorHamilton, NJFull timeAdditional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.
Actalent IncPart-Time Clinical Research Coordinator Actalent IncPart-Time Clinical Research Coordinatornew brunswick, NJ$25–$30 / hourQualifications:Minimum of one year of experience as a Clinical Research Coordinator or Community Outreach CoordinatorCommunity outreach experience requiredReliable transportationProficiency with electronic medical records (EMR) and electronic data capture (EDC) systemsPay and BenefitsThe pay range for this position is $25.00 - $30.00/hr. Key Responsibilities:Community Outreach: Visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.
Occupons QuebecRemote Market Research Assistant Earn Up to $50/Task Occupons QuebecRemote Market Research Assistant Earn Up to $50/TaskTrenton, NEW JERSEYRemoteYou will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
ETSAssociate Research Scientist ETSAssociate Research ScientistPrinceton, NJProvide scientific and technical skills so as to contribute to conceptualizing, designing, obtaining support for, conducting, and managing one or more of the following: (1) research projects or (2) development projects, particularly those for which scientific principles are applied to the creation of tools to improve the efficiency or quality of the practice of test development or statistical analysis; new item types; (3) the scoring of responses to open-ended items; (4) innovative assessment prototypes or products. Participate in dissemination activities through the publications of research papers in peer review journals and in the ETS Research Report series, the issuing of progress and technical reports, the presentation of seminars at major conferences and at ETS, or the use of other appropriate communication vehicles, including books and chapters, that impact practice in the field or at ETS.
Princeton UniversityNew***REVISED***** Postdoctoral Research Associate Princeton University***REVISED***** Postdoctoral Research AssociatePrinceton, NJI understand Princeton University expects all applicants to exhibit the highest level of integrity and ethical conduct, and that my concealment of any information, or my provision of misleading or false information, the University considers to be relevant will constitute grounds for it to cease the consideration of my employment or, if I am selected or hired, to withdraw or rescind my job offer or to terminate my employment, as applicable. Applications must be submitted online at https://www.princeton.edu/acad-positions/position/39502, and should include a cover letter, curriculum vitae that includes a list of publications, a brief statement (3 pages max) of research interests and goals and the names and contact information for three references.
Princeton UniversityResearch Assistant - Temporary Princeton UniversityResearch Assistant - TemporaryPrinceton, NJWith a collecting history that extends back to 1755, the Princeton University Art Museum is one of the leading university art museums in the country, featuring collections that have grown to include more than 117,000 works of art ranging from ancient to contemporary art and spanning the globe. The candidate will undertake research on the collections, provide support for projects related to the ancient Mediterranean collection, and will work collaboratively with the curator on exhibition projects that are underway.
Colgate-PalmoliveNewSr. Director, Clinical Research Colgate-PalmoliveSr. Director, Clinical ResearchPiscataway, NJ$250,000–$275,000 / yearDevelop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.
Princeton UniversityCollaborative Research Program Coordinator Princeton UniversityCollaborative Research Program CoordinatorPrinceton, NJ$80,000–$92,000 / yearA project management role will be required for collaborations as they arise, and the coordinator will assure that members of the Princeton community are aware of opportunities provided by the CTSA as they emerge, including restricted research grants, pilot project awards, workshops, and research facilities. The coordinator will also provide support to trainees (students and early-stage faculty) supported by the award, making them aware of research resources and educational opportunities, and facilitating interactions with the broader CTSA community at Princeton, Rutgers, and the CTSA Consortium.
Integrated Resources, IncScientist 2, Research & Development Integrated Resources, IncScientist 2, Research & DevelopmentSummit, NJContractorThis role focuses on the technical evaluation and execution of products in the Canadian market The Senior Scientist will have full responsibility for documentation and product development activities of mid-to-low complexity projects. Requirements: Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field Strong knowledge of formulation science, ingredients functionality and compliance, and consumer product market.
Magna-Power Electronics IncJunior Electronics Research & Development (R&D) Engineer Magna-Power Electronics IncJunior Electronics Research & Development (R&D) Engineerflemington, NJWith continued growth and recipient of the 2020 NJ Top Workplace 2021 Great Places to Work and 2022 Hunterdon County Business of the Year awards Magna-Power competes in a worldwide marketplace and addresses a broad range of applications including electric vehicle powertrain development and manufacturing particle accelerators semiconductor fabrication cutting-edge energy research national defense among many others. Magna-Power Electronics a Flemington New Jersey based electronics manufacturer is seeking an experienced Junior Electronics Research and Development R&D Engineer to join its dedicated world class team.
Rutgers The State University of New JerseyPostdoctoral Associate - Center for Healthy Aging Research (CHAR) Rutgers The State University of New JerseyPostdoctoral Associate - Center for Healthy Aging Research (CHAR)New Brunswick, NJAt a minimum, responsibilities will include: • Assisting with the design and execution of research studies • Analyzing datasets • Preparing manuscripts • Presenting findings at scientific conferences and local meetings • Assisting the PI with mentoring trainees as appropriate • Contributing to grant and fellowship applications • Collecting data and participating in community events associated with the labs research and mission. The specific benefits vary based on the position and may include: • Medical • Prescription drug • Dental coverage • Paid vacation • Holidays • Various leave programs • Competitive retirement benefits • Including defined contribution plans and voluntary tax-deferred savings options • Employee and dependent educational benefits when applicable • Life insurance coverage • Employee discount programs.
Rutgers The State University of New JerseyResearch Associate Position in Stem Cell Biology and Neuroscience Rutgers The State University of New JerseyResearch Associate Position in Stem Cell Biology and NeuroscienceNew Brunswick, NJWe use a wide range of multidisciplinary approaches, including: • Human pluripotent stem cell reprogramming and differentiation • CRISPR-Cas9-mediated genome editing • Electrophysiology and patch-clamp recordings • Advanced imaging techniques • Molecular and cellular biology • Biochemistry • Pharmacology • Bulk and single-cell RNA sequencing and data analysis • Transgenic and surgically induced animal models • Behavioral analyses. Certifications Licenses Required Knowledge, Skills, and Abilities We seek highly motivated candidates with expertise in one or more of the following areas: • Molecular biology and genome engineering, including CRISPR-Cas9-mediated gene editing • Electrophysiology, including patch-clamp recordings in brain slices or cultured cells • Bioinformatic and computational analyses, such as single-cell transcriptomic data analysis.
VitaliefClinical Research Nurse VitaliefClinical Research NurseNew Brunswick, NJFull timeDeliver high-quality, compassionate, hands-on oncology nursing care while coordinating closely with investigators, clinical teams, and ancillary departments (e.g., pathology, radiology, clinical laboratory, surgery, infusion services) in accordance with study protocols, treatment plans, and Good Clinical Practice (GCP) guidelines. IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR.
Rutgers The State University of New JerseyTenured or Tenure-Track Open Rank Faculty Position, Basic/Translational Science, in the Rutgers Addiction Research Center/ Brain Health Institute Rutgers The State University of New JerseyTenured or Tenure-Track Open Rank Faculty Position, Basic/Translational Science, in the Rutgers Addiction Research Center/ Brain Health InstitutePiscataway, NJ$120,000–$350,000 / yearPosting Summary The Brain Health Institute BHI https://brainhealthinstitute.rutgers.edu and Rutgers Addiction Research Center RARC https://addiction.rutgers.edu are recruiting a tenured or tenure track faculty member at Assistant/Associate Professor level to expand our research portfolio in the basic translational science of substance use disorders broadly defined to include preclinical or human subjects-based research programs. Posting Details Special Instructions to Applicants To become a part of our vibrant research community, applicants should submit a CV, cover letter, and a brief statement of research accomplishments and plans, one page maximum, to Dr. Chris Pierce and Dr. Anna Konova, Chairs of the search committee, at chris.piercerutgers.edu and anna.konovarutgers.edu.
Abacus Service CorporationScientist 2, Research & Development Abacus Service CorporationScientist 2, Research & DevelopmentSummit, NJBy applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. This role is pivotal in driving the technical evaluation and execution of products in the Canadian market, ensuring successful project launches.