• Oncology Early Stage Clinical Scientist (Director,…

    Pfizer (South San Francisco, CA)
    **POSITION SUMMARY** You will lead and coordinate the development of multiple studies of novel biological and small molecules for first in human (FIH), proof of ... in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead , coordinate,… more
    Pfizer (08/21/25)
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  • Oncology Early Stage Clinical Scientist Senior…

    Pfizer (Groton, CT)
    **POSITION SUMMARY** You will work collaboratively with the Global Development Lead (GDL) (and members of the development team) to establish, lead , coordinate, ... guidance from a more senior study clinician. Depending on experience, you may lead the development of the clinical protocol and may participate as an individual… more
    Pfizer (08/15/25)
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  • Clinical Development Physician, Oncology (Medical…

    Astellas Pharma (Northbrook, IL)
    …multiple early-phase programs in the Immuno-Oncology group. + Reports to the Medical Lead /disease area strategy head for the given program(s) and is accountable for ... closely with safety officer in writing and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events. +… more
    Astellas Pharma (08/29/25)
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  • Dean of the College of Engineering…

    University Of Vermont (Burlington, VT)
    …solvers, inspiring each other to build true world solutions that will lead to healthy, sustainable societies. The College offers modern facilities, focused energies, ... or institutions in the region. It is expected that the Dean will lead collaboration across departments and programs to ensure cohesion and to leverage intra-… more
    University Of Vermont (07/18/25)
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  • Director, Medical Affairs - US

    Organon & Co. (Jersey City, NJ)
    …the medical affairs organization and reports into the Contraception TA Lead /Global Director of Medical Affairs (GDMA). This role involves developing, updating, ... Contribute to the development of the global medical affairs plan (GMAP). + Lead REMS Medical Affairs activities: Serve as the Medical Affairs Contraception lead more
    Organon & Co. (09/12/25)
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  • Associate Director Clinical Compliance

    GRAIL (Durham, NC)
    …cross-functionally to proactively manage both GCP and CDx regulatory risks, lead inspection readiness, and continuously improve quality standards utilizing insights ... from inspections, audits, and evolving regulatory landscapes. **Responsibilities:** + Lead and manage internal processes and systems, clinical and diagnostic quality… more
    GRAIL (08/02/25)
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  • Executive Medical Director, Clinical Development

    Taiho Oncology (Pleasanton, CA)
    …work for those who need it most. This is an exciting opportunity to lead global clinical trials and experience multiple facets of Clinical Development in a dynamic, ... and accountable for program deliverables. Performance Objectives: + Medical global lead for development program(s) + Provide oversight for global Phase I-III… more
    Taiho Oncology (06/25/25)
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  • Global Senior Director Medical Affairs - Oncology…

    Merck (Rahway, NJ)
    …research, post-registration company-sponsored studies and areas of interest for the investigator -initiated study program (MISP) The Sr. GDMA chairs the Global ... works in close collaboration and alignment with the Value and Implementation lead . Support the Regional Directors Medical Affairs and other medical functions,… more
    Merck (09/12/25)
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  • Clinical Research Leader (PM) - Jjmt…

    J&J Family of Companies (Irvine, CA)
    …company personnel. + Lead all aspects of development and execution of Investigator agreements and trial payments. + Leads clinical data review to prepare data ... across the organization. **Key Responsibilities:** + Serve as a Clinical Research Lead to implement and run company sponsored clinical trials, ensuring compliance… more
    J&J Family of Companies (09/11/25)
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  • Clinical Research Associate - Clinical Research…

    Hartford HealthCare (Hartford, CT)
    …the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all activity associated with research study protocols. ... the SrCRA supervises HHC approved Research Volunteers. While the Principal Investigator is primarily responsible for the overall design, conduct, and management… more
    Hartford HealthCare (09/06/25)
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