• Senior Director- Clinical Design Program…

    Lilly (Indianapolis, IN)
    …statistical/inferential methods, rating instruments, regulatory standards, safety assessment, investigator /site management, decentralized clinical trials). + ... people who are determined to make life better for people around the world. Clinical Design provides clinical program and trial design leadership and expertise… more
    Lilly (11/12/25)
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  • Sr. Clinical Research Manager (DOM…

    Johns Hopkins University (Baltimore, MD)
    …assist regulatory staff with informed consent and protocol amendments for investigator -initiated studies + Manage clinical research budget generation and ... Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health… more
    Johns Hopkins University (11/08/25)
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  • Assoc Director Clinical Research…

    UT Health San Antonio (San Antonio, TX)
    …should have a track-record supportive of their filling the project Director or co- investigator leadership roles in clinical studies and projects with complex ... Assoc Director Clinical Research Informatics, Mobile Health San Antonio (https://uthscsa.referrals.selectminds.com/faculty/jobs/2749/other-jobs-matching/location-only)… more
    UT Health San Antonio (10/15/25)
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  • Lab Animal Technician II, Division of Laboratory…

    Wayne State University (Detroit, MI)
    …medications and treatments; collect laboratory samples as requested by principal investigator , clinical veterinarian or research personnel which requires ... utilizing a variety of medical apparatus and instruments, eg bandages, swabs, etc. Attend departmental staff meetings. Participate in continuing education and employee training programs. May require rotation through several on-campus and off-campus research… more
    Wayne State University (11/11/25)
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  • Associate Director, Regulatory CMC (Small…

    BeOne Medicines (San Mateo, CA)
    …product lifecycle for the assigned project. + Provide CMC regulatory review for clinical protocols and investigator brochures, etc. for the assigned project. + ... Provide comments on new global guidance through company's commenting process. **Supervisory Responsibilities:** The position may or may not manage direct report(s). **Computer Skills:** Microsoft 360, Familiarity with Veeva is a plus. **Qualifications:** + 8+… more
    BeOne Medicines (09/23/25)
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  • Scientific Director, Medical Affairs - Oncology

    AbbVie (Mettawa, IL)
    …design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and ... such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational… more
    AbbVie (11/06/25)
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  • Clinical Research Coordinator 2

    University of Miami (Miami, FL)
    …policy.5. Distributes study drug materials according to practice standards and clinical credentials as delegated bythe Principal Investigator .6. Monitors, ... Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Clinical Research Coordinator 2 to work at the UHealth Medical Campus in Miami,… more
    University of Miami (11/07/25)
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  • Physician - Internal Medicine - Breast Oncology…

    Rush University Medical Center (Chicago, IL)
    …multi-disciplinary breast oncology program, participate in our large portfolio of clinical trials, and develop investigator -initiated trials. The predominant ... Department: Internal Medicine **Work Type:** Full Time **Breast Oncology - Clinical Faculty** **Rush University Medical Center** **Chicago, IL** **Rush University… more
    Rush University Medical Center (11/27/25)
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  • Open Rank Faculty/Associate Director for Basic…

    University of North Carolina- Chapel Hill (Chapel Hill, NC)
    …duties include: upon request, perform reviews of grant applications and investigator -initiated clinical trials originating from the Center to ensure ... research. The AD BCR shall be an established, NCI funded independent investigator with interdisciplinary translational research in any area of cancer biology with… more
    University of North Carolina- Chapel Hill (09/01/25)
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  • Principal Medical Writer- FSP

    Parexel (Dover, DE)
    …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature ... comply with International Committee on Harmonization guidelines, Sponsor SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member,… more
    Parexel (10/11/25)
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