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The successful candidate will be instrumental in drug safety activities, supporting records management and compliance across clinical development and marketing programs. A minimum of 2 years of experience in a pharmaceutical industry setting within Drug safety, Pharmacovigilance, or equivalent.
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Comprehensive knowledge of biologic and drug development process, pharmaceutical technology, manufacturing processes, GMP, quality assurance & management and related issues, preferably in the areas of cell and gene therapy.
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Senior Drug Safety Specialist, Compliance - Contract - Cambridge, MA. Proclinical is on the lookout for a dedicated and experienced professional to fill the role of Drug Safety and Pharmacovigilance Compliance Specialist.
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The position will assist in biology assay development for both early and late-stage research programs focused on neurobiology and immunology drug discovery. Biological assay development to support early and late-stage drug discovery programs.
ExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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A minimum of 10 years of related pharmaceutical or biotechnology industry experience in clinical pharmacology, population PK, PK-PD modeling, DMPK, and/or pharmacometrics and a proven track record advancing programs through the drug development process, from discovery through IND to registration, informing data driven decisions on dose and schedule, making tough judgement calls where needed.
ExpandApply NowActive JobUpdated 9 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 4 days ago - UpvoteDownvoteShare Job
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The team is led by our CMO, a physician and medical oncologist with over 25 years of experience in large pharma and biotech drug development. Served as clinical and, ideally, strategic enterprise leader who has delivered in multiple phases of drug development (including clinical protocol development) and ability to deliver against challenging goals.
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PhD in Drug Metabolism, Pharmacokinetics, Chemistry or related scientific discipline with a minimum of 10 years of biotech/pharmaceutical drug discovery and development experience.
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Enanta is using its robust, chemistry-driven approach and drug discovery capabilities to become a leader in the discovery and development of small molecule drugs with an emphasis on indications in virology and immunology.
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Communicate with cross functional teams as DMPK project representative to advance projects through the drug development process. A track record of driving DMPK projects with a focus on drug disposition.
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The candidate will be responsible for formulation and process development activities of oligonucleotide drug product programs to support Biogen's growing pipeline. Biogen is presently looking to fill a Scientist II position within its Anti-Sense Oligonucleotide (ASO) Formulation and Drug Product Development group.
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Experience in the development of computational tools for drug design. BIOVIA is looking for a motivated Machine Learning Engineer – Drug Discovery to join our Discovery Studio team in San Diego, CA, or Waltham, MA in an onsite/hybrid role.
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We are seeking a highly motivated and skilled candidate to join Novartis Biomedical Research as a Discovery Postdoctoral Fellow within the Discovery Sciences (DSc) department to work on expanding the scope of covalent drug discovery.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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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 10 days ago - UpvoteDownvoteShare Job
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As a Senior Scientist, you will work within the RNA Medicine team to develop a novel nucleic acid drug development platform. Innovate: Lead multiple drug discovery and development projects.
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drug development jobs Company: Ppd in Boston, MA
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