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You will work with experienced pharmacometricians, Preclinical Pharmacokinetics, Drug Metabolism, Toxicology, and Clinical Pharmacology colleagues to provide inputs to overall product development plans and to address research and development objectives and issues.
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Oversees the design, conduct, and reporting of modeling and simulation analyses conducted by external Contract Research Organizations (CROs) in support of regulatory submissions. Experience in the preparation of components of the Clinical Pharmacology sections of Regulatory submissions for IND- and NDstage projects OR.
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Experience in optimizing and delivering peptide-protein conjugates as candidates for clinical trial. Seeking a highly motivated and talented peptide chemistry leader to join our new discovery peptide research group.
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A large Health system is looking for a Clinical EMR Trainer who will focus in Physician Training as well as Ancillary Services trainings. Serves as an active member as the Clinical EMR Trainer on hospital committees related to clinical education.
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DBMI has research and/or service programs in the following areas: Clinical informatics, clinical research informatics, biomedical data modeling and ontologies, biomedical natural language processing and information retrieval, medical artificial intelligence, privacy technology, global health informatics, equity in informatics, and translational bioinformatics.
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Current working knowledge of cellular and molecular immunology, cell biology, or related discipline, with an applied understanding of antibodies and antibody generation, biologics drug discovery research and disease target evaluation.
$108,000 - $139,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead projects and teams towards agreed upon goals, ultimately working towards clinical candidate peptide nomination. This BioPharma is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options.
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Interest or experience in environmental planning and regulatory compliance (California Environmental Quality Act, National Environmental Policy Act, and National Historic Preservation Act (Section 106) and historic preservation.
$65,820 - $111,894 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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SRCC works closely with Sponsored Research Development (preaward) and Sponsored Research Administration (post award), the Office of Technology Transfer, as well as SDSU's Research Support Services (compliance) to ensure that compliance, policies and procedures are adhered to in the negotiation and awarding processes.
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Contribute clinical pharmacology sections of clinical study protocols and reports and regulatory documents including Investigator Brochures, IND, and BLA/IMPDs, etc. PhD, PharmD or equivalent in Pharmacokinetics, Pharmacology, Bioanalytical or related field with at least 5+ years of experience in Clinical Pharmacology, DMPK or related disciplines required.
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A bilingual Licensed Clinical Social Worker, Licensed Professional Counselor, or Licensed Psychologist is sought to work as a primary care team member and provide short-term clinical behavioral health consultation services in a fast-paced setting.
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Near-term focus will be on leading the legal support for supply chain, clinical trials and regulatory issues and will evolve to also include supporting commercialization capabilities. + Collaborate with the BMS Law Department on IP issues, trademarks, data privacy, regulatory and GXP and compliance issues.
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Strong scientific and business acumen - the ideal candidate will have in-depth medical, scientific, regulatory, and technical knowledge of most functional areas involved in drug discovery, platform and/or clinical drug development.
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Human Longevity, Inc. (HLI), is a privately held human health information technology and health care company founded by pioneers in the fields of genomics and stem cell therapy to revolutionize human health and the practice of medicine.
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Sample Management : Establish and manage a biomarker sample storage and inventory plan, including identifying third-party vendors, ensuring regulatory compliance, and developing a sample database and tracking system in collaboration with biology, clinical science, and bioinformatics teams.
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clinical research pharmaceutical company regulatory compliance jobs Title: senior director in San Diego, CA
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