• Associate Director, Digital Strategy & Data…

    Lilly (Indianapolis, IN)
    …least 5 years ofproject management. Minimum of5 years of experience in pharmaceutical , biotechnology , or other FDA-regulated industries with deep understanding ... manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow… more
    Lilly (11/18/25)
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  • Senior Quality Assurance Specialist

    Curia (Rensselaer, NY)
    …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Join our talented workforce, where a ... a related field + Minimum 8 years QA, RA or Compliance experience in pharmaceutical industry (preferred in APIs) at USFDA regulated facilities + Broad knowledge of… more
    Curia (09/24/25)
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  • Summer Intern PhD Student Drug Delivery

    Bristol Myers Squibb (New Brunswick, NJ)
    …currently enrolled in an accredited university program seeking a Ph.D. in Pharmaceutical Science, Pharmaceutical Chemistry, Biotechnology , Chemical or ... Self-motivated and highly self-driven individuals are required. Prior drug product development research experience is a plus. **The program will feature** : + An… more
    Bristol Myers Squibb (11/24/25)
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  • Clinical Development Lead Prostate (Acp3)

    Bristol Myers Squibb (San Diego, CA)
    …and other site personnel involved in clinical trials. + Skilled in clinical research and understand the process of pharmaceutical product development and ... Lead Prostate (ACP3)** RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on… more
    Bristol Myers Squibb (11/19/25)
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  • Head of Data and AI Enablement, R&D DD&T (Vice…

    Takeda Pharmaceuticals (Boston, MA)
    …progressive leadership in digital, data, technology, or R&D roles within global pharmaceutical , biotechnology , or healthcare organizations. + Proven track record ... tremendous opportunity for a leader who thrives in a global, regulated pharmaceutical environment and is passionate about delivering impact at scale. **Key… more
    Takeda Pharmaceuticals (11/07/25)
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  • Associate Director, Compensation

    Mitsubishi Chemical Group (Jersey City, NJ)
    …Our parent company - one of Japan's most respected - is a research -driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global ... for inter-cultural norms and management practices. + Prior experience in the pharmaceutical , biotechnology or similar industry is preferred. + Proven knowledge… more
    Mitsubishi Chemical Group (10/18/25)
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  • Regulatory Coordinator - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. ... direction of the Breast Oncology Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office… more
    Dana-Farber Cancer Institute (11/26/25)
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  • Development Scientist, Oncology Clinical…

    Astellas Pharma (Northbrook, IL)
    …is acceptable. + Thorough knowledge and demonstrated expertise in biotechnology / pharmaceutical industry related to clinical drug development (early-stage ... of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We… more
    Astellas Pharma (11/27/25)
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  • Manager, Medical Affairs Strategy

    IQVIA (New York, NY)
    …medical treatments. Our diverse client base includes the global top 20 pharmaceutical , medical device, and biotechnology companies as well as healthcare ... is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With direct access to the… more
    IQVIA (11/04/25)
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  • FSP Senior Epidemiologist (Inflammation)

    IQVIA (Wayne, PA)
    …of four (4) years of relevant post-doctoral experience, preferably in pharmaceutical industry, biotechnology , or consulting environment. Master's degree in ... comparators, benchmarking of clinical outcomes, comparative safety and effectiveness research , and post-authorization studies + Lead development of study protocols,… more
    IQVIA (10/29/25)
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