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Under general direction, the Microbiologist II performs moderate to highly complex laboratory testing and analysis on bacterial and fungal isolates to provide information to the SENTRY program, new drug development protocols and clinical trial protocols.
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An individual at the level of Principal Scientist, Oral Formulation Development will be expected to either lead projects and innovations as an individual contributor or to build and lead a team focused on oral formulation development for small molecule and peptide drug products and amorphous intermediates.
$145,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Ph. D. with at least four years of pharmaceutical drug development experience relating to: PKPD, pharmacometrics, mathematics, statistics/ biostatistics, or chemical/biomedical engineering.
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We're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint.
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Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.
$64,000 - $128,000 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Karuna is seeking an experienced and motivated individual to join our Quality Assurance team as Manager/Senior Manager, CMC Quality Assurance, to support drug development from Phase 1 to commercialization.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Familiarity with HVAC wiring diagrams Highly organized and motivated Excellent communication skills Strong troubleshooting and problem-solving skills Possess and maintain a valid driver’s license Must pass a pre-employment background check and drug screen Benefits Unlimited earning potential.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Counseling and Human Services (CHS) Chair oversees the Licensed Professional Counselors (LPC) program, the Counselor Education (COUN) program, Clinical Mental Health Counseling (CMHC) program, Criminology, Law & Society (CLS) programs, and Drug and Alcohol Counseling (DAAC) program.
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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.
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Minimum 5 years of employment in clinical development, drug safety or regulatory or equivalent. Experience in drug development. They will be responsible for leading all interactions regarding product safety issues with Research and Development (R&D) governance committees and regulatory agencies.
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Education:Required: MD, DO, or equivalentPreferred: Board CertificationRequired Experience and Skills:Minimum 3 years clinical practice experience following post-graduate medical trainingExperience in drug developmentMinimum 3 years of experience in clinical safety, pharmacovigilance and/or risk managementMinimum 5 years of employment in clinical development, drug safety or regulatory or equivalentDemonstrated organizational leadership skills, preferably in the employment areas noted above.
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There may be opportunity to rotate to another area in Clinical Drug Development or Global Medical/Scientific Affairs after the first year. The program provides in-depth exposure to clinical drug development with emphasis on key elements of clinical trial planning, execution, data analysis and reporting of clinical trial results.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Knowledge of Good Clinical Practices ICH/GCP, drug development process, regulatory requirements for the conduct of high-quality clinical trials including protocol development, medical review, oversight of study conduct, data quality and safety is preferred.
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At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - from clinical trial support to real-world evidence generation. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - from clinical trial support to real-world evidence generation.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Contribute to the development of NGS assays to benefit drug discovery and translational research. Demonstrated expertise in molecular biology techniques, including DNA/RNA extraction & purification, NGS library preparation & QC, PCR, qPCR, etc.
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