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Director/Sr. Director - Process DevelopmentGreater Boston Area Competitive Compensation + excellent bonus/benefitsDuties and Responsibilities:Lead all process development activities (cell culture/banking/development, fermentation, protein purification, tech transfers)Oversee internal(in-house) and external vendors (domestic & international CDMOs)Work cross-functionally with CMC & Manufacturing leaders such as Analytical, Drug Product, QA/QC, Manufacturing, Supply Chain, etc.
$210,000 - $240,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Data collection and analysis; development and maintenance of project timelines; statistical issues in clinical trials; describing advanced statistical techniques and interpreting results; regulatory/research guidelines on drug development, GCP, and statistical principles (including ICH guidelines); SAS programming; and budget review and input.
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C4T’s degrader medicines are designed to harness the body’s natural protein recycling system to rapidly degrade disease-causing proteins, offering the potential to overcome drug resistance, drug undruggable targets and improve patient outcomes.
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Albertsons Companies is a leading food and drug retailer in the United States. The Company operates stores across 34 states and the District of Columbia with 24 banners including Albertsons, Safeway, Vons, Jewel-Osco, Shaw's, Acme, Tom Thumb, Randalls, United Supermarkets, Pavilions, Star Market, Haggen, Carrs, Kings Food Markets and Balducci's Food Lovers Market.
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Working knowledge of drug development, clinical research, study design, biostatistics, pharmacokinetics, the regulatory environment, and medical terminology. What you will do: Work with and lead project teams to prepare clinical documents, including but not limited to protocols, CSRs, and IBs to support drug development.
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Experience in academic or industry research required - direct experience in drug discovery or translational/clinical research experience is a plus. Familiarity with diverse methods and recent technological advances in neuroscience research.
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Aegis delivers evidence-based, clinically actionable information related to medication compliance, substance abuse, and drug-drug interactions through definitive testing of urine, oral fluid, or blood specimens.
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Licensure as a Alcohol and Drug Counselor (LADC I or LADC II), Certified Addictions Counselor (CAC), or Certified Alcohol and Drug Abuse Counselor (CADAC) preferred. Licensure as a Alcohol and Drug Counselor (LADC I or LADC II), Certified Addictions Counselor (CAC), or Certified Alcohol and Drug Abuse Counselor (CADAC) preferred.
$26 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the SR Director, Drug Product as part the CMC Technical Operations team the Principal Scientist, Drug Product, will provide strategic and technical leadership within the CMC Technical Operations to support the development and optimization of Akebia's clinical and commercial programs.
$185,119 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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A thorough understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing. Knowledge of GLP/GCLP and GCP global regulatory requirements for clinical trial submissions (USA, UK & EU), understanding of 21CFR Pt. 11 with respect to clinical systems (QMS.
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Current research at RAND focuses on a broad array of topics, including mental health services research, health care, drug policy, disaster recovery, and homeland/national security. PhD in criminology, criminal justice, or relevant discipline (you may also apply if you are at the dissertation stageand expect to complete your PhD within 12 months); or PhD in other discipline or JD with evidence of extensive application of research methods to behavioral or social science issues; or Master‘s degree in public policy, public health, or a technical discipline with 5+ years experience and demonstrable research leadership and proficiency in research methods.
$262,500Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Types of cases include:·violence in the workplace·substance abuse·abusive conduct·asset or drug diversion·compliance and privacy breach ·harassment·discrimination based on protected classes·conflict resolution.
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Deep understanding of drug discovery processes, covering both small molecules and biologics drug discovery, Strong background on chemistry, pharmacology, DMPK, toxicology for IND enabling is a plus.
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This is an excellent opportunity for a motivated drug developer to shape the Hematology pipeline at VCGT and lead innovative pre-clinical and clinical stage cell and gene therapy programs. Job DescriptionGeneral Summary:Vertex/VCGT (Cell and Gene Therapy) is searching for an experienced Senior Medical Director for a leadership role in managing assets in its hematology development portfolio, specifically including sickle cell disease and beta-thalassemia.
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Advanced degree in a biologic/medical/clinical/nursing field: Pharmacist/PharmD, Nurse Practitioner or PhD with at least 7 years experience in drug safety and risk management within the pharmaceutical, biotech or CRO industry.
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drug job in Watertown, MA
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