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Founded in 2015, the company has built a portfolio of 20+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
InternExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Preferred Drug Development knowledge with understanding of other functions relevant to the position which may include: Research, Preclinical, Clinical, Manufacturing, Commercial and Regulatory.
$200ExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Sares Regis Group of Newport Beach, California, is a privately held real estate development, investment and management firm that focuses on commercial properties and multifamily communities in the western U.S. Since its founding in 1993, SRG has developed and acquired more than $7 billion in commercial and residential assets.
$22.75 - $24 an hourFull-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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PhD in pharmaceutical sciences, engineering, statistics, mathematics, or a drug development-related field with 12+ years of experience in the pharmaceutical or biotechnology industry. A broad understanding of drug development as evidenced by a track record of significant contributions to successful Regulatory Agency interactions, NDAs and/or BLAs, drug approvals, in-licensing deals, and peer reviewed publications.
$220,000 - $330,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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We are seeking a Bioinformatics Data Engineer to spearhead the development of an AI-first ecosystem aimed at transforming the drug discovery landscape. Passion for Innovation: A strong passion for using AI to drive innovations in health technology and drug discovery.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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A strong passion for using AI to drive innovations in health technology and drug discovery. Collaborate on Drug Discovery Strategies: Work with interdisciplinary teams to translate experimental data into actionable drug discovery strategies.
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This position will support drug development in diverse therapeutic areas such as inflammation, fibrosis, oncology, and virology. The successful candidate will provide scientific and technical overview for tissue-based methods that span sample processing, assay development, whole slide scanning, image QC, analysis, and data reporting.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Demonstrates knowledge of global clinical trials and the drug development process, Knowledge of IRT system setup and functionality and proficiency with Excel modeling, Strong collaboration and excellent team skills to be successful in cross-functional and multi-cultural teams.
ExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Works collaboratively with Clinical Operations, Formulation Process Development, Device Development and Clinical Package Engineering, Quality Assurance, Regulatory, Outsourced Manufacturing and Project Management partners to develop optimal supply strategies and ensure on time delivery of clinical supplies to initiate and resupply studies with investigational medicinal product (IMP.
$74 - $82 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are seeking an innovative and motivated Senior Scientist I to develop and implement novel capabilities and assays to functionally characterize our therapeutic antibody drug candidates and to help spearhead projects to continually improve and expand upon our internal capabilities.
$130,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are looking for a candidate who is experienced in cell therapy drug development in an biotechnology setting. The Regulatory Affairs & Quality Assurance Lead will support U.S. regulatory activities related to our cellular therapy programs, including the planning, development and execution of regulatory submissions and the overseeing of CMC Regulatory and Quality Assurance activities.
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5+ years of experience in drug discovery with proven leadership of preclinical development of therapeutic project(s) and clinical candidate selection is a requirement. Experience as a project team lead (PTL) in a drug discovery setting for biologics programs.
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Has significant industry knowledge, including knowledge of drug development, and is able to flex own knowledge to work on molecule and/or non-molecule projects. Interacts with other functions across Development and Research (key contacts include ClinPharm Rep, Bioanalysis Rep, ClinPharm Management, Clinical Operations, Clinical Data Science and Regulatory Affairs.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Understands the life sciences industry (e.g., CROs, pharma/biotech, medical device), scientific & clinical data/terminology, and the drug development process. This position is primarily remote, non-office based, with the expectation to travel up to 50.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The successful candidate will have strong technical skills with a background in cancer immunology, and will be expected to work in a fast-paced, nimble startup, and effectively collaborate with colleagues across scientific teams to advance preclinical drug development.
Full-timeExpandApply NowActive JobUpdated 1 month ago
drug development jobs in San Carlos, CA
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