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As an Oncology Clinical Research Coordinator (CRC), you will be an integral part of studies at Astera Cancer Care by recruiting participants, collecting and managing the study data for the successful management of clinical trials.

Job Description:.

Colgate-Palmolive Co logo

Piscataway, NJ26 days ago
  • $250,000–$275,000 Per Year

p>Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci Sakir, Suavitel, PCA SKIN, EltaMD, Filorga and Hello as well as Hill's Science Diet and Hill's Prescription Diet.

  • Develop 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.

    • New York, NY25 days ago

    Job Summary/Basic Function: Primarily, the research assistant will conduct hands-on coding and data analysis of qualitative and quantitative data collected from multiple impact evaluations under the supervision of a senior research scientist and/or PI. CPRE researchers have made their mark studying the effectiveness of federal, state, and local policies, with particular emphasis on accountability systems, school finance, teacher quality initiatives, assessment systems, and school governance.

    NJ30+ days ago
    • $310,900–$489,400 Per Year

    li>

    Working closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility.

  • Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.

    • Rahway, NJ10 days ago
    • $282,200–$444,200 Per Year

    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.

    • Rahway, NJ15 days ago
    • $173,200–$272,600 Per Year

    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 and/or Associate Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility.

    The Senior 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.

    Rahway, NJ30+ days ago
    • $282,200–$444,200 Per Year

    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.

    Rahway, NJ30+ days ago
    • $282,200–$444,200 Per Year

    The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area.

    Rahway, NJ15 days ago
    • $282,200–$444,200 Per Year

    li>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.

    The Senior 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.

    New York, NY30+ days ago
    • $42,100–$42,100

    em>For more information, go tomed.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, TwitterandInstagram.

    Prior experience in clinical research, healthcare, scribing, patient interaction, or an academic health system setting
    Experience with REDCap, Epic, or similar research and clinical data systems
    Interest in orthopedics, surgery, translational research, or patient outcomes research
    Current gap-year status or intention to apply to medical school or other health professional programs
    Coursework in anatomy, physiology, medical terminology, or related clinical sciences

    Qualified candidates must be able to effectively communicate with all levels of the organization..

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