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We are seeking an experienced and highly motivated Associate Director of Analytical Development to manage and drive analytical development and quality control activities across our small molecule drug discovery and development programs.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We’re seeking a Business Development leader in biotech or pharma to play a leadership role in developing and executing our business strategy of Twist Antibody Drug discovery capabilities and expanding our growth and value creation opportunities including partnerships, alliances, out-licensing deals and other collaborations.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Director of Radiopharmaceutical Process Development will be executing the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead purification process development and transfer to internal and contract manufacturing facilities to produce GMP and non GMP drug substances on time and with high success rate. Well versed in FDA, EMA and ICH guidelines relating to registration, quality, and compliance concerning drug substance and authored CMC sections in commercial filings (BLA, MAA) and post approval changes.
$307,560ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director, Chemical Development & Drug Substance Manufacturing is self-motivated and demonstrates initiative in responsibilities and always strives to do the job better. Successful candidate will be passionate about synthetic chemistry, excited to solve complex problems in a fast-paced environment, and comfortable in the multidisciplinary environment of drug development research.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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By broadening the covalent drug universe with lysine-targeted chemistry, it becomes possible to remove even the most devastating disease-driving proteins, dramatically improve current medicines and create new therapies with optimized clinical profiles.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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They will apply scientific training and clinical research experience to support all aspects of drug development, from facilitating the transition of molecules from pre-clinical discovery through the achievement of clinical proof of concept and to supporting the registration and commercialization of a product.
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This role provides scientific expertise in solid oral dosage formulation development, late-stage process development, oversight of GMP drug product manufacturing at contract development sites, authoring global regulatory filings (INDs, IMPDs, etc.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Strong knowledge of GMP quality systems and regulatory requirements for drug development. In this pivotal role, you will lead their analytical development function, ensuring the highest standards of quality and regulatory compliance for their drug substance and drug product activities.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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PharmD or PhD in clinical research or clinical pharmacology with 8+ years' scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.
$307,560 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Partner seamlessly with program management, biometrics, regulatory, clinical operations, development sciences, drug safety, and other development functions to ensure successful delivery of the development program and filing activities.
$375,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Overseeing drug substance process development and manufacturing. Your responsibilities will include driving the development and manufacturing of drug substances, overseeing both internal and external resources, and collaborating closely with CDMOs to ensure the successful progression of our innovative compounds.
$185,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Leads clinical and/or disease strategy development, collaborating with a variety of internal and external partners and stakeholders, such as clinical investigators, scientists, and key opinion leaders, as well as multidisciplinary internal groups, including other groups in global functions such as research, clinical operations, drug safety, regulatory, portfolio management, business development, Product Development, market planning, legal, etc.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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MD or equivalent with 4+ years’ clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment. Provides ongoing medical monitoring for clinical trials, including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance.
$321,090 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In this role, you will lead and coordinate Packaging Process Validation, Packaging and Device Components Qualifications, upcoming Commercial Support, Process Monitoring, Deviations/CAPA’s and Close Collaboration with Drug Product Manufacturing and Combination Products Development team.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
drug job Title: development director in Burlingame, CA
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