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Research Jobs in Morgan, NJ

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:.

30+ days ago

New York, NY

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.

24 days ago

Somerset, New Jersey

b>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.. RESPONSIBILITIES:

  • Support Phase II–IV oncology clinical trials (pharmaceutical, ECOG, and PI-initiated studies); disease groups include Breast oncology, with expanding Lung, GI, and GU program.

15 days ago

Rahway, NJ
  • $282,200–$444,200 / 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.

    • 9 days ago

    NJ
    • $310,900–$489,400 / 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.

    • 30+ days ago

    Rahway, NJ
    • $173,200–$272,600 / 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.

    14 days ago

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