• Post Doctoral Fellow (Dr. Meng Zhang's Lab - SOM:…

    Emory Healthcare/Emory University (Atlanta, GA)
    …through non-canonical translation) role and regulation in aggressive prostate cancer; 2 ) Deciphering the epigenetic mechanisms of oncogenic gene upregulation driven ... specified field while receiving advanced training from a designated Principal Investigator to enhance professional skills and research independence needed for… more
    Emory Healthcare/Emory University (12/10/25)
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  • Customer Service Rep II

    TEKsystems (Indianapolis, IN)
    …when appropriate resolution is incomplete * Acting as a liaison for both internal and external clients * Communicating investigator site needs when new ... Experience in the pharmaceutical industry is an advantage * Notifying investigator sites, sponsors, and affiliates of laboratory results, sponsor determined flags,… more
    TEKsystems (12/08/25)
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  • Clinical Trials Manager - Center…

    Mount Sinai Health System (New York, NY)
    …or research operations within a hospital, academic center, or CRO, including 2 years in a management/leadership role required. + Experience in cardiovascular ... + Maintain the Trial Master File (TMF) and site investigator files in inspection-ready status. + Monitor study enrollment,...and data accuracy to ensure high-quality deliverables. + Lead internal and external audit readiness and serve as primary… more
    Mount Sinai Health System (11/25/25)
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  • Clinical Research Coordinator II (IITs)

    Loyola University Chicago (Chicago, IL)
    …with the Coordinating Center. + In collaboration with the Principal Investigator (PI) and Manager, will develop Study operations manual, data collections ... forms, case reports and other source documents for Investigator initiated Studies. + In collaboration with the PI...equivalent training acquired via work experience or education. + 2 - 5 years of previous job-related experience. +… more
    Loyola University Chicago (11/11/25)
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  • Clinical Research Coordinator II, Critical Care

    Beth Israel Lahey Health (Burlington, MA)
    …contracts with physicians and nurses and knowledge of the protocol. (essential) 2 . Checks all eligibility and ineligibility criteria with the research subjects' ... record. Verifies information with clinical research nurse and/or principal investigator . (essential) 3. Discusses informed consent with research subjects. Interacts… more
    Beth Israel Lahey Health (10/30/25)
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  • Clinical Research Coordinator

    University of Utah (Salt Lake City, UT)
    …control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in ... of study related documentation; prepares reports for organizations and agencies. 2 . Develops study budgets; monitors budget expenses and billing for allied… more
    University of Utah (10/25/25)
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  • Medical Science Liaison - Gastroenterology…

    Sanofi Group (Cambridge, MA)
    …unmet needs. + Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial ... and enhance discussions with key stakeholders. **Collaborates effectively with internal stakeholders** + Distribute relevant scientific and medical information and… more
    Sanofi Group (11/14/25)
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  • Regional Medical Affairs Director

    Xeris Pharmaceuticals, Inc. (GU)
    …clinical research, and real-world experience/evidence. RMADs are recognized as an internal subject matter expert and provide appropriate medical and scientific ... support for internal teams as identified. **Candidate to reside in Houston,...to Xeris clinical research activity, including thought leader and investigator engagement and follow-up, and facilitation of unsolicited requests… more
    Xeris Pharmaceuticals, Inc. (12/04/25)
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  • Clinical Trials Regulatory Specialist III | School…

    Emory Healthcare/Emory University (Atlanta, GA)
    …regulatory guidance on study development. + Liaison between the sponsor, the investigator , Winship, Emory IRBs, external IRBs and internal departments/staff. + ... to multiphase) and manage the study activation process. + Serves as the internal project manager for assigned specific oncology disease group(s), providing the group… more
    Emory Healthcare/Emory University (11/22/25)
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  • Manager, Medical Writing (Remote)

    Teva Pharmaceuticals (West Chester, PA)
    …and edits clinical regulatory documents (eg, study reports, protocols, briefing books, investigator 's brochures, health authority responses, Module 2 .5 and 2 ... experience, Lead author experience in: Protocols/protocol amendments, Clinical study reports, Investigator 's brochures, Clinical summary documents (Modules 2 .5, … more
    Teva Pharmaceuticals (12/09/25)
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