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A New Jersey licensed professional counselor, or licensed marriage and family therapist, who is a certified clinical supervisor by The Certification Board, A New Jersey licensed physician, certified by the American Society of Addiction Medicine, or a Board-certified psychiatrist; or a New Jersey licensed advanced practice nurse who is a certified clinical supervisor by the Certification Board, h.
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Reports to a Manager (or above) within NACD. Manages mutually beneficial relationships with external partners relevant to the planning and implementation of clinical trials improvement/innovation projects for NACD and Novo Nordisk (e.g., clinical trial site staff, IRBs, clinical research vendors.
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Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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Familiarity with EDC, IRT, eTMF, CTMS, SAS, Argus, clinical analytics, safety, LMS, QMS, TraceLink, Veeva Vault and/or regulatory systems. Solid domain knowledge of business processes and related data types in functional areas (Pre-clinical, clinical development, clinical operations, regulatory, pharmacovigilance, biostatistics, data management, quality, and manufacturing), to support technology solutions.
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The Senior Clinical Trial Physician, Rheumatology sits within Cell Therapy Clinical Development, which is a global organization dedicated to the effective design and execution of drug development.
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Quantitative Systems Pharmacology (QSP) & Physiologically Based Pharmacokinetics (PBPK) have become important components of discovery and clinical development. Desire to interact as a modeling and simulation expert with matrix project teams and working closely with experts from different functional areas (pre-clinical and clinical and multiple therapeutic areas.
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Design and develop translational medicine and clinical biomarker strategies in collaboration with team members to inform and enable the clinical development of Hematology-Oncology program(s.
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In our state-of-the-art histology and immunohistochemistry laboratory, you'll support a variety of programs, ranging from discovery to clinical trials, all aimed at advancing antibody therapeutics.
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Oversee the incorporation of new technology and innovation (biostatistics, digital biomarkers, data management, eConsent, eMedical Records ) in clinical trial quality. Demonstrated strong knowledge of ICH/GCP, regulatory guidelines/directives, clinical research processes and principles of Quality Assurance.
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Clinical biomarker evaluations are integral to the success of our precision medicine, tumor agnostic approach. In collaboration with Clinical Development, Biostatistics, Clinical Pharmacology, and Translational Medicine, develops a biomarker analysis plan to support clinical studies, as appropriate.
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A PhD in oncology/immuno-oncology, or related field, with at least eight (8) or more years of translational research, applicable biomarker, and/or clinical trial experience. The TM team focuses on preclinical and clinical translational research to advance the clinical development of innovative and differentiated antibody therapeutics for the treatment of cancer.
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We are actively looking to hire talented PMHNP-BCs in the Manalapan, NJ area who are passionate about patient care and committed to clinical excellence. You'll see clients in an outpatient clinical setting either in-person or via telehealth.
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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
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As a passionate and experienced Board-Certified Behavior Analyst (BCBA) looking to elevate your career to the next level, you’ll join Kaleidoscope ABA Therapy as a Clinical Manager and lead a team of dedicated BCBAs in creating a positive and transformative impact.
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In-depth knowledge of clinical pharmacology, PK, PD, drug metabolism, biopharmaceutics, and bioanalytical chemistry. PhD in Clinical Pharmacology (or a related area such as pharmacokinetics, pharmacology, pharmaceutics) with a minimum of 10 years of experience in these areas.
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