• Regulatory Coordinator - Gynecologic Oncology

    Dana-Farber Cancer Institute (Brookline, MA)
    … Trials Office to complete the regulatory requirements of the GYN Oncology clinical research project . The RC coordinates aspects of protocol submissions, ... Office for Human Research Studies (OHRS), Office of Data Quality (ODQ) and the Clinical Trials Offices...and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and… more
    Dana-Farber Cancer Institute (07/23/25)
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  • Associate Manager, Data Validation Engineer

    Takeda Pharmaceuticals (Boston, MA)
    …members of Clinical Study teams to foster an environment of quality and efficient specifications and documentation to support audit-readiness and ICH compliance. ... compliance with trial master file requirements. Contribute to the successful conduct of Takeda's clinical trials and to the delivery of high- quality data in a… more
    Takeda Pharmaceuticals (07/12/25)
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  • Head of Bioinformatics

    Sanofi Group (Cambridge, MA)
    …Biology Cluster is seeking a highly motivated Head of Bioinformatics to lead efforts in advancing discovery of novel targets and therapeutic opportunities, based ... of multi-modal disease data (including but not limited to genetics, genomics, cellular, clinical and pathological disease data). The ideal candidate is a proven … more
    Sanofi Group (08/17/25)
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  • Executive Director, Pathology, BIDMC

    Beth Israel Lahey Health (Boston, MA)
    …experienced healthcare leader and is responsible for all technical operational, clinical , and financial performance for BIDMC Pathology. The ED is involved with ... to support the future needs of BIDMC. Expected to lead , serve, and participate in various committees at the...Supervises and directs the work of all operational and quality pathology leaders at BIDMC. Plans, organizes, manages and… more
    Beth Israel Lahey Health (07/02/25)
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  • GMP Account Specialist - Cell Solutions (Remote)

    Charles River Laboratories (Wilmington, MA)
    …get POs for GMP opportunities. * Act as a GMP key liaison/business development leader for assigned territories not currently managed by a BDE. * Develop and deliver ... team developing initiatives including GMP-focused webinars, campaign follow-ups, and lead generation programs. * Coordinate cross-functional collaboration with Client… more
    Charles River Laboratories (08/21/25)
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  • Senior Scientist, Global Biologics

    Takeda Pharmaceuticals (Boston, MA)
    …throughput and data quality . + Contributes to multiple projects, interfacing with project teams to meet timelines for project progression. + Represents the ... therapeutics to support Takeda's pipeline and advance novel therapeutics into clinical development in Takeda's three therapeutic areas of interest: Oncology… more
    Takeda Pharmaceuticals (06/25/25)
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  • Operations Associate Cardiac Monitor Tech, Full…

    Baystate Health (Springfield, MA)
    **Baystate Health, a nationally recognized leader in healthcare quality and safety, is looking for a Full Time Operations Associate/Cardiac Monitor Technician to ... Springfield, MA **THE ADVANTAGES OF WORKING WITH BAYSTATE!** + Excellent Compensation High- quality , low-cost medical, dental and vision insurance + Generous PTO - up… more
    Baystate Health (08/21/25)
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  • Associate Director, Statistics

    Takeda Pharmaceuticals (Boston, MA)
    …at the program level. + Contribute to representing data science function on project teams in support of pre- clinical and clinical studies ... to enable quantitative decision making from target identification through lead optimization + Contributing statistical modeling expertise to cross-functional … more
    Takeda Pharmaceuticals (05/31/25)
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  • Scientist/Sr. Scientist, Translational Development

    Bristol Myers Squibb (Cambridge, MA)
    …there is an opportunity for a dynamic and resourceful individual to lead a team of innovative laboratory scientists that are addressing scientific questions ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
    Bristol Myers Squibb (08/21/25)
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  • Principal Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    …Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight for critical new product development ... lifecycle ensuring that requirements are maintained. Identify risks within regulatory strategies, project plan, and outline proposal for balancing the project more
    Philips (06/28/25)
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