• Regulatory Investigator

    The City of Houston (Houston, TX)
    REGULATORY INVESTIGATOR Print (https://www.governmentjobs.com/careers/houston/jobs/newprint/5176973) Apply  REGULATORY INVESTIGATOR Salary $18.20 - ... OVERVIEW Applications accepted from: ALL PERSONS INTERESTED Job Classification: REGULATORY INVESTIGATOR Posting Number: 37836 Department: Administration &… more
    The City of Houston (12/20/25)
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  • Environmental Investigator II/…

    The City of Houston (Houston, TX)
    Environmental Investigator II/ Regulatory Compliance Print (https://www.governmentjobs.com/careers/houston/jobs/newprint/5160349) Apply  Environmental ... Investigator II/ Regulatory Compliance Salary $2,085.89 - $2,259.00 Biweekly Location Houston, TX Job Type Full Time Job Number 37711 Department Houston Public… more
    The City of Houston (12/23/25)
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  • Associate Director, Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …reportable events. They will oversee the organization and maintenance of all regulatory affairs documentation/ investigator site files (ISF) as required by ... programs and resources, and much more. Posted Job Title Associate Director, Regulatory Job Profile Title Associate Director, Clinical Research Regulatory Job… more
    University of Pennsylvania (10/09/25)
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  • Clinical Research Regulatory Coordinator

    Rush University Medical Center (Chicago, IL)
    …group studies, single site studies, intergroup studies, industry studies, and investigator initiated studies. Prepares internal and external regulatory ... and investigator initiated studies. * Writes and prepares IRB regulatory submissions, including but not limited to consent forms, new project applications,… more
    Rush University Medical Center (11/26/25)
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  • Regulatory Coordinator - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …Coordinators (RC)** works under the direction of the Breast Oncology Principal Investigator (s), Regulatory Operations Manager, Clinical Research Manager and / or ... directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project. The RC coordinates aspects of protocol submissions,… more
    Dana-Farber Cancer Institute (11/26/25)
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  • Clinical Research Physician

    Lilly (Boston, MA)
    …+ Serve as a key medical expert in cross-functional discussions, including regulatory submissions, investigator meetings, and advisory boards. + Work with ... strategic leadership throughout the trial lifecycle, ensuring scientific integrity, regulatory compliance, and patient safety. You will collaborate with… more
    Lilly (12/12/25)
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  • Director, Clinical Development (MD)

    Gilead Sciences, Inc. (Foster City, CA)
    …+ Manages the clinical development component(s) in the preparation/review of regulatory documents, investigator brochures and development plans. + Coordinates ... Presents scientific information at scientific conferences as well as clinical study investigator meetings. + Adheres to regulatory requirements of study conduct… more
    Gilead Sciences, Inc. (11/14/25)
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  • Regulatory Specialist C

    University of Pennsylvania (Philadelphia, PA)
    …C functions independently with minimal supervision on complex protocols that are Investigator Initiated. The Regulatory Affairs Specialist C authors and conducts ... regulatory assessments of core documents (protocols, Informed Consents, investigator brochure, etc), and is responsible for leading and drafting IND briefing… more
    University of Pennsylvania (10/09/25)
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  • Regulatory Affairs Specialist-CC

    University of Pennsylvania (Philadelphia, PA)
    …forms and source document tools, as well as, to provide direct regulatory /compliance guidance and facilitate investigator -initiated trials and investigator ... and wellness programs and resources, and much more. Posted Job Title Regulatory Affairs Specialist-CC Job Profile Title Clinical Research Regulatory Specialist… more
    University of Pennsylvania (12/14/25)
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  • Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …safety signals. + Review documents supporting clinical development such as Investigator 's brochure, regulatory documents for IND/CTA, clinical sections of ... Lead, Clinical Scientist. and other functional areas such as GCO, biostats, regulatory , pharmacovigilance. The Director will be a key contributor to INDs, NDAs,… more
    Teva Pharmaceuticals (10/07/25)
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