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Principal Scientist, Clinical Pharmacology, Modeling & Simulation page is loaded Principal Scientist, Clinical Pharmacology, Modeling & Simulation Apply remote type Flex Commuter / Hybrid locations US - California - South San Francisco time type Full time posted on Posted 7 Days Ago job requisition id R-181781 Career Category Scientific Job Description HOW MIGHT YOU DEFY IMAGINATION.
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In-depth knowledge of clinical trial process, EDC systems (i.e., Medidata Rave, InForm, etc.) The Sr. Director, Clinical Data Management (CDM) will be responsible for the operational and strategic aspects of data management across the organization, including data governance, data quality, and data strategy.
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In this vital role you will be responsible for the development and implementation of the Quantitative Clinical Pharmacology, Modeling and Simulation strategies for cutting-edge novel modalities including Bi-specific T-cell engagers, Bi-specific antibodies, oncolytic viruses, antibody-drug-conjugates, CAR-T cells-based therapies in addition to small molecule & mono-clonal antibodies.
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The Clinical research Coordinator (CRC) will perform independently or with general direction at the fully operational level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI; Dr. Golden); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
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Ambience Healthcare was founded after 2.5 years of R&D in large language model (LLM) technology to address one of the most impactful productivity opportunities in healthcare: clinical documentation.
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Provide leadership to early-stage clinical scientists on the clinical study team for Early Clinical Development, working in a matrix team environment with other clinicians, statisticians, clinical pharmacologists, translational biologists, drug safety/pharmacovigilance, clinical supply, and regulatory specialists.
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Jump-start your career as a(an) Clinical Pharmacist Specialist today with Methodist Hospital. You will lead and develop pharmacy clinical services such as drug consults, nutrition support, pharmacokinetics, anticoagulant monitoring, pain management, IV to PO, renal dosing and other programs as defined by Pharmacy Leadership.
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Under the supervision of a Clinical Research Coordinator (CRC) or Principal Investigator (PI), the Assistant Clinical Research Coordinator will perform entry-level duties related to the support and coordination of several research studies, primarily the study “ Reimagining Precision Medicine Approaches to Alzheimer’s Disease Diagnosis.
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The Sr. Clinical Data Manager will be responsible to support all aspects of data management from study start-up to database lock including EDC design, data review/cleaning, query management, data reconciliation, and data transfer specifications.
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Top biopharma sponsors, clinical research organizations, healthcare providers and institutions rely on ConcertAI’s evidence-generation and digital transformation capabilities to advance precision medicine and medical innovation.
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Additionally, the Clinical Procurement Coordinator supports donor families, provides family care and may provide families with the option of organ and/or tissue donation. The Clinical Procurement Coordinator is responsible for response to donor referrals, donor evaluation, and donor management, coordination of organ recovery, organ preservation, and organ distribution.
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ConcertAIs leading real-world evidence, AI technology and software-as-a-service solutions support healthcare decision-making across clinical research & development through commercialization. Contribute to discussions with internal and external stakeholders in the design, analysis, and interpretation of clinical real world evidence studies.
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Coordinates cross-functional data review meetings with the clinical team. Knowledge of ICH GCP and Good Clinical Data Management guidelines. Reviews clinical data and metrics to identify data quality trends, compliance with the protocol, consistency of data across subjects and sites and potential risks to timelines.
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Under the direction of the Pediatric Cellular Therapy Laboratory (PCTL) Senior Supervisor, the Clinical Lab Scientist Supervisor has leadership responsibility and appropriate authority for administrative and fiscal functions as assigned.
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We’re seeking an experienced Senior Clinical Research Associate to join the Veterinary Operations team that achieves its mission through developing veterinary partnerships, engaging with the veterinary community through education, ensuring excellence in the science behind our products, executing clinical trials and studies.
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Title: clinical Company: F Hoffmann La Roche in South San Francisco, CA
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