• Novo Nordisk Inc. (Boulder, CO)
    …is responsible for the production of non-cGMP oligonucleotide API to support toxicology studies . In addition to ensuring the supply of API and meeting production ... goals, the Specialist, API Manufacturing actively supports continuous improvement initiatives and identifies wherever possible improvements that reduce risk and cost to the overall operation. Relationships Specialist, API Manufacturing reports to the Senior… more
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  • Merck & Co. (North Wales, PA)
    …well as statistical support for translational oncology projects and studies .-Interact with Clinical, Regulatory, Statistical Programming, Data Management, and other ... company Research Laboratories scientists in designing and analyzing data from clinical trials as well as analyzing oncology biomarker and clinical data.-Coordinate all statistical activities for ongoing clinical projects.Education Requirements:-PhD in… more
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  • Merck & Co. (North Wales, PA)
    …communicate and implement lessons learned across sites, regions and studies Position Qualifications: Education Minimum Requirements: Bachelor's degree + 5 ... years OR Master's + 3 years Pharmaceutical and/or clinical drug development experience OR PhD/PharmD Degree in life sciences, preferred. Required Experience and Skills:Pharmaceutical and/or clinical drug development experience.Excellent oral (including… more
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  • Lovelace Biomedical Research Institute (Albuquerque, NM)
    …from and administers agents to research animals as IACUC approved studies require. Documents laboratory work to acceptable standards and maintains laboratory/medical ... equipment and supplies in accordance with Standard Operating Procedures (SOPs), protocols and regulations. The successful candidate will assist in administrative functions of study execution such as labeling collection tubes and transporting supplies to… more
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  • Lovelace Biomedical Research Institute (Albuquerque, NM)
    …collects samples from and administers agents to research animals as IACUC approved studies require. Works with a variety of animal species and tasks will involve ... both in-vivo and in-vitro procedures.Documents laboratory work to acceptable standards and maintains laboratory/medical equipment and supplies in accordance with Standard Operating Procedures (SOPs), protocols and regulations. The successful candidate will… more
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …with regulatory requirements among project team members and across all studies .Review deliverables before transfer to either internal or external clients ensuring ... quality.Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.Education Qualifications (from an accredited college or university)Bachelor's Degree requiredMaster's Degree… more
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  • Merck & Co. (Rahway, NJ)
    …quantities of life-changing medicines.Design and conduct lab and/or pilot-scale studies to support mechanistic understanding, scale-up, and transfer of processes ... to manufacturing. Collaboration and effective communication: Work with a collaborative, cross-functional team of talented scientists and engineers to advance the biologics pipeline from early- to late-stage development.Partner with groups in both research and… more
    HireLifeScience (06/04/24)
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  • Aequor (South San Francisco, CA)
    …research group). Responsibilities are primarily carrying out animal research studies , including monitoring, dosing, and animal necropsy and organ collection. ... Primarily in mice, with occasional work in rats and guinea pigs. The individual may need to work with infectious and/or bio-hazardous reagents and material. The individual will be involved with general lab managerial duties such as stocking and ordering… more
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …novel therapeutics Provide clinical and scientific expertise to the design of studies , writing of protocols and other study and regulatory-related documents for ... DCR-PHXC, and other programs Participate in the analysis and interpretation of data, ensure integrity of trial data, and assist in reporting of study results including preparation of scientific summaries, abstracts and manuscripts Provide leadership in the… more
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  • Merck & Co. (Durham, NC)
    …molecule purification (chromatography, filtration) or bio-analytical assays.Ability to drive studies and experiments in the context of a long-term commercialization ... plan.Ability to provide scientific mentorship and guidance to technical colleagues.Take lead in solving technical problems and equipment issues.Proficient using statistical tools (JMP or Minitab) for experimental design, data analysis and modeling.Experience… more
    HireLifeScience (06/04/24)
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