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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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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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We are a research site, working to develop therapeutic ADC drug candidates for clinical testing. Senior Research Associate I, BioconjugationPosition Summary:Catalent Pharma Solutions in Emeryville, CA is seeking a Sr. Research Associate I who will be responsible for the conjugation, purification, and HPLC (high-performance liquid chromatography) analysis of site-specific antibody-drug conjugates (ADCs.
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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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This will include but are not limited to: bull Recording scientific observations during gross examinations Excising weighing and fixating tissues during necropsy Maintenance of study records bull Quality control of work and entering data in the department database Coordinating study logistics The candidate will also be executing and coordinating the logistics of pathology samples for non-clinical studies conducted at Client.
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Design, development and optimization of existing and new analysis techniques and metrology solutions to support research, process/IP development and failure analysis on our cutting-edge scd wafer technology.
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Ability to think outside the box and bring new ideas and thinking to the UX Research space. Advanced understanding of UX Research methods with the ability to articulate study design to stakeholders.
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Identify laboratories to publish abstracts working with Scientific Affairs in support of Hologic Diagnostic products and product launches. + Provide support for internal Digital Cytology studies to support product research and design and as needed/requested.
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Immediate need for a talented Translational Research Scientist - II (Associate). Familiarity with computer software: Illumina BaseSpace, Omicsoft, TIBCO Spotfire, Graphpad Prism, Ingenuity Pathway Analysis, Geneious.
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Demonstrated knowledge and experience in establishing bioanalytical methods, ADME, PK/PD for a variety of therapeutic modalities, ideally in both preclinical and clinical environment. Provide scientific DMPK leadership and strategic direction to research project teams.
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The position also collaborates with the other psychotherapists to implement and sustain best practices in the area of integrative psychotherapy and guided imagery, and to stay abreast of research and best practice in the field of behavioral health and integrative medicine.
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This position may have clinical responsibilities at both the San Francisco and Oakland campuses and would actively contribute to the Department’s mission of excellence in research, education, and patient care.
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About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease.
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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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Perform and report on litigation history research regarding opposing parties and counsel. Perform Daubert research regarding party experts using publicly available data and other research tools.
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clinical research affairs jobs Company: Biophase in San Francisco, CA
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