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This position requires a Ph. D, with a strong scientific background in Oncology research (basic and/or clinical). The postdoctoral fellow will work closely with the OED safety team as well as other cross functional members of the oncology early development team (e.g. preclinical safety and toxicology, discovery, pharmacology and pharmacokinetics, regulatory, statistics) bridging preclinical/discovery expertise to the very early phases of clinical safety (e.g. pre-IND interactions, and IND submission and initial FIH phase.
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5+ years of experience in clinical science, clinical research, or equivalent. + Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
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You will deploy and deliver technical solutions at the intersection of computational chemistry and machine learning, supporting research directions in molecular design across broader gRED and Roche.
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Areas of direct responsibility include Perioperative Services, Clinical Services (Pharmacy, Lab, and Radiology), Facilities, Supply Chain, Major Construction, Patient Experience, Clinical Technologies and Nursing Education.
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The Principal Scientist will be Subject Matter Expert who will apply innovative Quantitative Clinical Pharmacology approaches to guide optimal drug development including. Experience in leading the design and implementation of clinical pharmacology and biopharmaceutic studies including bioequivalence, bio-comparability, drug-drug interaction, special population, ethnic sensitivity, ADME and pediatric studies and integrating results into regulatory filings, and product labels.
$142,936 - $171,592 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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You will be a part of a highly collaborative and dynamic research environment where we aim to translate our understanding of cancer biology to develop personalized therapies and diagnostics to transform clinical practice to benefit patient health.
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The candidate will be expected to collaborate with Medicinal Chemistry and Pharmacology to develop and implement studies vital to address key program DMPK issues and successfully advance research compounds into development.
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2 years of experience in leadership experience working in an Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC) accredited animal research facility. Works closely with Cedars’ Facilities Management and Research Facilities Operations to identify, report and follow up on maintenance and repairs under their purview.
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Apply now and make a significant impact on the future of clinical trials and biomarker research! Exciting Opportunity: Seeking Senior Data Scientist (Fully Remote)Location: Remote Competitive Pay Rate: $89/hr - $91/hr Are you a highly motivated Data Scientist looking to make a significant impact in the field of clinical trials and biomarker data.
$89 - $91 an hourFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Kelly® Science & Clinical is seeking a Clinical Research Psychometric Rater and Manager for a fulltime, direct hire position with a pharmaceutical client in South San Fran, CA. 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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Who We Are The Government Programs (GP) Team within Channel and Contract Management is responsible for managing the complexities of Government Contracting and Price Reporting to enable patient access through the federal drug programs (Medicare, Medicaid, 340B, Veterans Affairs and Department of Defense Federal Supply Schedule & TRICARE.
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Must be Licensed Clinical Psychologist with the CA BOP. Collaborate with our dedicated provider support team, our licensed clinical care navigation team, and our administrative care support team.
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The Study Manager will work cross-functionally with internal program teams and CROs. Responsibilities Primarily responsible for selecting, contracting, and monitoring non-GLP and GLP nonclinical studies with Contract Research Organizations (CROs), expert consultants and academic collaborators.
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CERTIFICATION & LICENSURE: Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement Practitioner (CDIP)Certified Coding Specialist (CCS) or Certified Professional Coder (CPC)SKILLS AND KNOWLEDGE:Knowledge of Pathophysiology and Disease Processes sufficient to pass the clinical pre-employment test at a rate of 85% or better is required for new hires.
$63.74 - $95.6 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Preferred Qualifications: Experience with cell culture and molecular research techniques including but not limited to DNA cloning and isolation, PCR, RNA isolation, RT-PCR, protein isolation, and western blot analysis.
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clinical research affairs jobs Title: director Company: Biophase in Brisbane, CA
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