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Evaluate and develop the most appropriate biochemical and biophysical characterization tools to support biological drug product development, including adjuvanted vaccine drug products.
$152,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Reporting to the Director, Project Management, the Associate Director, Project Management is responsible for managing cross-functional drug development projects, in either preclinical or clinical development stages.
$150,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
$180,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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10 years or more of experience in pharmaceutical clinical drug development in industry including protocol development; study initiation and follow-up; IRB/EC submissions and interactions; review of clinical study data listings; review and/or preparation of clinical study reports.
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Global BDO Strategy to Improve Drug Development: Primarily participates and may occasionally lead moderately complex initiatives, with some level of supervision, to improve the harmonization and efficiency of drug development which leads to cost savings and shortened timelines for the company.
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Each plan includes 100% coverage for preventive care, telemedicine through Teledoc, prescription drug coverage, and behavioral health coverage. The Clinical Nurse is responsible for his/her own professional development, including licensure, Basic Life Support (BLS) certification, and maintaining current knowledge regarding the assigned patient population.
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Extensive knowledge of ICH GCP, other relevant ICH guidelines and regulatory requirements (minimally US FDA) regarding applicable drug development regulations. Support the development and maintenance of applicable Quality Systems and procedures that comply with applicable GCP standards and guidelines.
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At Databricks, we are inspired by allowing data teams to solve the world’s toughest problems, from security threat detection to cancer drug development. More than 10,000 organizations worldwide — including Comcast, Condé Nast, Grammarly, and over 50% of the Fortune 500 — rely on the Databricks Data Intelligence Platform to unify and democratize data, analytics and AI. Databricks is headquartered in San Francisco, with offices around the globe and was founded by the original creators of Lakehouse, Apache Spark, Delta Lake and MLflow.
$192,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Minimum of ten years of relevant work experience in the biotechnology and/or pharmaceutical industry; of which a minimum of five years working in a project management role, preferably working with multi-disciplinary drug development teams.
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Significant experience participating in cross-functional projects and teams with responsibilities related to clinical trials, or other drug development activities. Thorough knowledge of the drug development process, including all key functions involved in the various stages of drug development from early research through post-marketing.
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Experience in Phase III drug development GxP environment and commercial operations. Develop and communicate corporate compliance policies and standards for GMP operations and partner with peers in clinical operations to support the development and maintenance of similar documents for GVP, GLP, and GCP operations.
$185,000 - $230,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Thorough understanding of the drug development process, clinical trial methodology, regulatory requirements, and GCP. Acquires and enhances knowledge related to drug development, clinical trials methodology, and DM best practices, and applies the information to make recommendations for improvement to processes and business performance.
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This Ecosystem Business Development role will focus on bringing our AI protein generation platform to a wide range of industrial and academic partners in the global market. We are committed to achieving breakthroughs in target discovery and drug design, and bringing global first-in-class medicine for unmet medical needs in the areas of immune oncology, autoimmune diseases, fibrosis, and aging-related diseases.
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Excellent working knowledge of clinical pharmacology (pharmacokinetics, pharmacodynamics, translational medicine) and drug development principles. 8+ years of biotech/pharma drug development experience with deep expertise in clinical pharmacology.
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This will include diverse therapeutic modalities (e.g., small molecules, biologics, oligonucleotides) and novel laboratory and digital biomarkers, developed internally and in-licensed; all development stages (focus is IND/CTA through clinical proof-of-concept); diverse regulatory pathways; and regulatory elements of key drug development functions (e.
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drug development jobs in Palo Alto, CA
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