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MD with 10+ years of experience in drug development and drug safety/pharmacovigilance, with specific expertise in clinical oncology, immunology, or genetics. Job Overview: This position is well-suited for a Medical Director with substantial expertise in drug development and safety, providing a unique opportunity to strategize the implementation of safety surveillance for clinical trials, oversee the management of safety signals, take charge of cross-functional teams, and contribute to the development of regulatory safety deliverables.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Our Small Molecule Drug Substance Development and Manufacturing team has an opportunity for Scientist position to support our small molecule drug development pipeline. Work in a team of Arcus scientists and partner contract development and manufacturing organization teams to develop efficient manufacturing processes for small molecule drug substance preparation under GMP. The projects may encompass clinical stage candidates through commercial launch.
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As a Clinical Pharmacologist, the Associate Director/Director will be responsible for designing, conducting, and analyzing clinical pharmacology studies, as well as providing expert advice on pharmacokinetic and pharmacodynamic aspects of drug development and regulatory submissions.
$125,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Since integrating into Lundbeck in October 2019, Lu-SBP has supported commercial launch of Lundbeck's first biologic product (Vyepti) and advancement of a growing biologics pipeline in collaboration with our Copenhagen-based Process Science & Validation Team. The Lu-SBP team leads and supports the development of new product candidates from cell line development through commercial validation of Drug Substance and Drug Product manufacturing processes.
$20 - $22 an hourInternExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Hold a PhD (or Master's) in Pharmacology, Pharmaceutical Sciences, Oncology, Toxicology, or a related field, with at least 2 years of pertinent experience (or 5+ years for non-PhD candidates), or possess an equivalent blend of industry expertise in preclinical drug discovery and development.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Demonstrated hands-on experience in assay development, especially for SEC, icIEF, CE-SDS, HIC, and residual-free drug analysis, is desired Experience in 2D-LC method development is a plus Experience in protein structural elucidation and peak identification using high-resolution mass spectrometry is a plus Experience in interfacing with CDMO/CTL for clinical or commercial biological products development is a plus Experience in method transfer and GMP qualification/validation is a plus.
$125,000 - $176,500 a yearExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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As a CMC development lead, the individual will apply their strong expertise in CMC fermentation and/or purification to develop robust, phase-appropriate processes for drug substance GMP production to enable human clinical studies and eventual licensure.
$200,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Your primary mission as Senior Scientist, Preclinical Development is to design and oversee experiments for validation (proof of concept) and development (IND enablement), and lead our Preclinical team’s operations to maximize scientific rigor in our drug discovery process.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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An exciting opportunity has risen for a Senior Pharmacologist to join a highly specialised contract research organisation providing pre-clinical bioassay services to support drug development programmes across pharmaceuticals and biotech companies.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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This position reports to the head of clinical pharmacology and toxicology and liaises with clinical development, clinical operations, non-clinical pharmacology and toxicology, and drug discovery to execute activities for advancing the development pipeline.
$150,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Senior Principal Scientist will collaborate across BMS sites with Analytical, Drug Product, Drug Substance, Quality, and Regulatory leads to execute drug product formulation/process development support, analytical strategies for drug product methods and specifications, analytical control strategies, and support of product development up to drug application submissions and approval.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Conduct laboratory research related to drug delivery, development of nanoparticle-based formulations, and characterizations for, but not limited to Ocugens products. The role of Research Scientist, Drug Delivery & Nanotechnology involves leading and conducting experiments for the discovery and preclinical activities of Ocugens product pipeline related to nanoparticle-based drug substances.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience in luminescence based and qPCR assay development, optimization, and high throughput screening in the context of small molecule drug discovery programs. Lead and contribute to project teams focused on target selection, target validation, lead generation and lead optimization to enable delivery of novel drug candidates into clinical development.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Biologics Analytical R&D (ARD) group develops antibody drug conjugates (ADC) and other therapeutic biologic medicines by developing analytical methods and providing analytical results to support drug substance and drug product process and formulation development.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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It has expertise in biomarker development, disease biology research and in the application of immunology and data science technologies to support drug discovery and development. R&D Strong knowledge and understanding of clinical drug development strategic planning of clinical research, ICF, ICH GCP, GLP is strongly preferred.
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drug development jobs Company: Genoskin
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