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Job Overview Explore research careers and be a part of something bigger! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. What you will be doing As a Study Technician Trainee you'll apply your scientific curiosity in researching the effectiveness, safety and toxicity of drugs in early de
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Organizes and conducts routine and non routine sample analysis in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. Documents work and maintains study documentation and laboratory records. Performs QC review of data. Sets up, operates and performs routine and non routine maintenance on general equipment. Provides input and participates in project meetings, plan
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Contribute to architectural vision for Labcorp Drug Development's data architecture, data integration and master data management strategies. Design and implement core ETL workflows for Labcorp Drug Development's information integration and reporting infrastructure. Participate in the development of APIs and integration. Participate in the full development cycle from product inception, research and
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Job Overview We are hiring a Medical Technologist II for our Vaccines team in Indianapolis, IN ! ($5000 Sign On Bonus and Relocation Provided exclusions may apply ) Essential Functions Quality Control Monitoring Programs o Review and investigate unacceptable results to internal and external quality control monitoring programs. Prepare corrective action responses by assigned due date for management
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Job Overview Labcorp Drug Development has a dynamic REMOTE (US based) position for a Senior Contract Specialist . We are looking for someone with passion for CTA work along with growing desire to achieve in the research and development space. In this role, you will ensure SOPs are adhered to, identify escalations, follow compliance standards, and update appropriate departmental contract tracking s
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Job Overview Labcorp Drug Development, a global contract research organization, has worked on all of the top 50 best selling drugs available today through its full spectrum of nonclinical, clinical and commercialization services with our clients from leading pharma and agile biotech. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of
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Job Overview Labcorp Drug Development is seeking candidates for a QA Compliance Lead Auditor. The QA Compliance Lead Auditor will be remotely located (home based) anywhere within the United Sates. Conduct work as identified on the audit activity table (listing on table is not all inclusive but a representative sample) Takes lead in generation of global QA policies on interpretation/ application of
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Job Overview Oversees designated global audit programs for compliance to the master audit plan (procedures, execution, QC, compliance to process, etc.) Identifies the scope and leads global audits and associated audit team Facilitates prioritization of global projects for risk based audits Ensure the consistent implementation, use and review of SOPs Escalate issues to management in a timely manner
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Job Overview We have an exciting opportunity for upcoming December 2021 or May 2022 grads to join our Immunology and Immunotoxicology team in Madison, WI or Greenfield, IN! Company Overview At Labcorp , we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions because we know that knowledge has the potential
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Method Development (MD) Act on the behalf of the method development Critical Reagent Inventory (CRI) owners to generate sub aliquots in e workbook, create labels in nautilus and take care of all labeling requirements Creates CRIs on behalf of method developers for new clients during method development Establish appropriate low inventory flag thresholds for all reagents through interaction with the
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Job Overview Labcorp Drug Development is seeking candidates for a Manager, Regulatory Submissions. The Manager, Regulatory Submissions will be remotely (home based) located anywhere within the United States or Canada. The Manager, Regulatory Submissions will be responsible for ensuring the timely submissions of appropriate documentation to Regulatory Authorities globally prior to the performance o
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Document work properly and maintain study documentation and laboratory records. Recognizes deviations from expected results and notifies line management. Operates equipment/instrumentation in accordance with appropriate SOPs. Effectively plans assigned workload on a daily basis Maintains a clean and safe laboratory work environment. Contributes to a cohesive team environment. Plans individual work
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Job Overview Senior Clinical Scientist Oncology Clinical Trial Mgmt and Medical Monitoring experience is required Remote in the USA or Canada Position leads Phase 1 3 Clinical Trials and oversees medical monitoring. This is not a laboratory/research scientist role. Why settle for one thing when you can have everything ? Covance by Labcorp gives you the best two for one opportunity for career growt
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Job Overview The Senior Manager QA Process Lead position is an individual contributor that has responsibility for oversight and delivery of the Internal Process Compliance function activities. This position and department will be aligned as partners to the functional areas of the Clinical Development and Commercialization Services (CDCS) business to ensure appropriate quality/compliance oversight
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Ensure that the Quality System is compliant with domestic and international quality system regulations (21 CFR 820; ISO 13485). Promote awareness of the Quality System and provide training to individuals across the organization on quality management principles, tools, techniques and best practices. Support the implementation of corporate policies and procedures relating to quality, design control,
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