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Responsibilities Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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Kelly® Science & Clinical is seeking a Regulatory Affairs Associate for 1 year contract position (with possibility of extension) position at a premier client in Skillman, NJ. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
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Responsible for the production of clinical supplies Review Literature and gather patent and published articles on the selected projects. On-Board Scientific is hiring a Formulation Scientist based out of New Brunswick NJ.
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No Relocation Assistance Offered# 159791 - Piscataway, New Jersey, United States Our company invites applications for the Sr. Research Scientist/Principal Scientist position, Dermal Clinical Research, Personal Care/Skin Health based in our Piscataway, New Jersey location.
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The OpportunityQuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
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Patient Mix: 11 bed unit with IMC/Tele; Hematology/oncology, chemo, autologous bone marrow transplant and CAR-T (Stem cell) overflow, bone marrow biopsy, new leukemia inductions, multiple transfusions, count recovery, and clinical trials.
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Allowing the new graduate nurse to gain clinical competency and achieve transition from student to professional practice. As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health.
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Develops, authors and executes study protocols and amendments by literature investigation, database searches and other existing/investigational products, liaising with key opinion leaders (KOLs), clinical trial investigators and internal scientific, pharmacology and regulatory teams.
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May also perform general administrative assistance including but not limited to opening, closing and maintaining the office, clubhouse and amenities, maintaining office organization and file structure, logging and retrieving customer packages.
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Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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Under the direct supervision of the PCMH Care Coordinator (PCC) or Site Manager and under a matrix system of supervision and guidance of the Director of Nursing, the Certified Medical Assistant (CMA) assists patients and their families in all aspects of their clinical interaction with their provider.
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Comprehensive cancer center: onsite imaging, rehab, nutrition, genetic counselors, radiology, and surgical support, and clinical trials. Opportunity to participate in high-quality clinical trials.
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Independently perform biologics assays on monoclonal antibodies, fusion proteins, antibody-drug conjugates (ADCs) and fixed drug ratio combination (FDRC) products to support clinical development of therapies, particularly against immuno-oncology (IO) and oncology diseases.
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Participates in clinical activities (i.e. assists with patient flow/care, helps to optimize throughput of patients via Radiology Ambassador team. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
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The candidate will be responsible in the purification of 50L to 1000L volumes engineering, clinical and commercial batches in a cGMP environment. Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation.
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clinical trial file jobs Title: trial master in Somerset, NJ
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