• Merck & Co. (Rahway, NJ)
    … supply chain across the full of our Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, ... at clinical development related meetings (i .e., Clinical Trial Team s ) and product...supplies . Interacts with key partner organizations such as clinical development, regulatory , quality and other supply… more
    HireLifeScience (01/16/25)
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  • Clinical Research Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The...regulatory aspects of the initiation of Phase I-V clinical trials with a focus on required… more
    University of Pennsylvania (12/13/24)
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  • Clinical Research Regulatory

    University of Southern California (Los Angeles, CA)
    … SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research- Regulatory - Specialist ... information pertinent to studying milestone progress, including but not limited to: clinical trial management systems, IRB databases, internal and external… more
    University of Southern California (12/12/24)
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  • Clinical Research Program Specialist

    Johns Hopkins University (Baltimore, MD)
    …**_Clinical Research Regulatory Specialist_** who will be responsible for managing regulatory start-up of clinical trials , assisting development of ... policies, standard operating procedures, and guidelines related to the conduct of clinical trials are followed. _Equipment, Machine, or Tool Requirements_ +… more
    Johns Hopkins University (01/07/25)
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  • Regulatory Specialist - CRI

    Methodist Health System (Dallas, TX)
    clinical , investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, ... requirements * Obtain and facilitate tracking of relevant regulatory documents for clinical trials ...trials assigned. * Assist in the development of clinical trial documents for signature of principal… more
    Methodist Health System (01/11/25)
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  • Regulatory Specialist

    Stanford University (Stanford, CA)
    …of hematopoietic cell transplantation for patients worldwide. BMT-CT is seeking a Clinical Trials Regulatory II Specialist to support a very active ... Regulatory Specialist **School of Medicine, Stanford,... Regulatory Specialist **School of Medicine, Stanford, California, United States**...clinical trials faculty. The position will anticipate and generate reports… more
    Stanford University (11/13/24)
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  • Veeva Quality Assurance Specialist

    University of Pennsylvania (Philadelphia, PA)
    …Title Veeva Quality Assurance Specialist (Abramson Cancer Center) Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The ... is a world leader in developing and conducting innovative clinical trials for the prevention, diagnosis, and...CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to… more
    University of Pennsylvania (12/08/24)
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  • Regulatory Specialist - Stephenson…

    Beth Israel Lahey Health (Boston, MA)
    …Word, Excel, PowerPoint or Access. **Preferred Qualifications:** + 1-3 years of clinical trial regulatory affairs experience preferred. **Competencies:** ... a difference in people's lives.** The Regulatory Specialist supports regulatory compliance for clinical...local bio safety committees on oncology human gene transfer trials . + Act as a liaison between the IRB… more
    Beth Israel Lahey Health (12/10/24)
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  • Clinical Research Coordinator (Full-Time)

    Hackensack Meridian Health (Hackensack, NJ)
    …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant… more
    Hackensack Meridian Health (01/14/25)
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  • Clinical Research Coordinator

    Hackensack Meridian Health (Hackensack, NJ)
    …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant… more
    Hackensack Meridian Health (01/21/25)
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  • Clinical Trials Specialist

    University of Washington (Seattle, WA)
    …in the Division of Hematology and Oncology, has an outstanding opportunity for a Clinical Trials Specialist (CTS) to join their team.** **POSITION PURPOSE** ... reports to the Senior Research Implementation Manager and Lead Clinical Trial Specialist . This position...assistance and in a resourceful manner to expedite opening clinical trials . This position interacts with representatives… more
    University of Washington (01/01/25)
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  • Sr. Sponsored Programs Specialist

    University of Miami (Miami, FL)
    …Department of SCCC has an exciting opportunity for a Full Time Sr. Sponsored Programs Specialist ( Clinical Trials Finance) to work at UHealth Medical Campus ... collaborative environment. Department Specific Functions Dept. Summary The Sr. Sponsored Programs Specialist ( Clinical Trials Finance) manages activities in… more
    University of Miami (12/19/24)
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  • Clinical Trials Applications…

    AdventHealth (Orlando, FL)
    ** Clinical Trials Applications Specialist II - AdventHealth Orlando** **All the benefits and perks you need for you and your family:** - Benefits from Day ... 125,000 outpatients each year **The role you'll contribute:** The Clinical Trials Application Specialist II...Specialist II is knowledgeable in the areas of clinical trial budgets and protocols, Medicare coverage… more
    AdventHealth (11/26/24)
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  • Clinical Trials Research Coverage…

    Rush University Medical Center (Chicago, IL)
    …and accurate coverage analyses with budget overlay in a timely manner. * Review clinical trial protocols and related regulatory documents to prepare a ... of each case. **Summary:** Reporting to the Director/Manager of Clinical Trials Research Revenue Cycle, this position...position will create coverage analyses in accordance with Medicare's Clinical Trial Policy (NCD 310.1) and assist… more
    Rush University Medical Center (11/21/24)
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  • Clinical Research Regulatory Project…

    Dignity Health (Phoenix, AZ)
    …Manages the daily operation and supervision of the Clinical Research Regulatory Affairs area and program specialist (s) in accordance with all applicable ... initiation and monitoring visits performed by pharmaceutical and device manufacturing clinical trial sponsors. Responsibilities Include: + Manages all functions… more
    Dignity Health (12/16/24)
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  • Regulatory Specialist

    UPMC (Pittsburgh, PA)
    regulatory portion of the trial submission process, and to maintain the regulatory integrity of assigned clinical trials from approval to closure ... UPMC Hillman Cancer Center is currently hiring a regular full-time Regulatory Specialist to help support the Oncology Clinical Research Services team located… more
    UPMC (01/08/25)
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  • Senior Regulatory Specialist

    UPMC (Pittsburgh, PA)
    regulatory portion of the trial submission process, and to maintain the regulatory integrity of assigned clinical trials from approval to closure ... Regulatory Specialist 's purpose is to develop regulatory forms/documents using assigned clinical study materials,...by adherence to ethical practices during the conduct of clinical trials to protect the rights and… more
    UPMC (12/07/24)
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  • Pre-Award Specialist Open Rank

    University of Colorado (Aurora, CO)
    …**Additional Duties for Level III** + Train oncology clinical trial budget Specialist I the clinical trials management software, OnCore TM + Train ... oncology clinical trial budget Specialist I budget management and...Award Specialist I:** + Experience working with clinical trials management software, preferably OnCore TM… more
    University of Colorado (01/16/25)
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  • Regulatory Compliance Specialist

    Houston Methodist (Houston, TX)
    …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... Compliance Specialist will be responsible for the Regulatory Binder for each clinical research study...from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research… more
    Houston Methodist (01/06/25)
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  • CTRP Specialist and PRMS Associate

    University of Southern California (Los Angeles, CA)
    …tools, which help patients, physicians, and the public identify clinical trials . The CTRP also supports regulatory compliance and facilitates the ... PRMS Associate to join its team. Job Summary: The Clinical Trials Reporting Program (CTRP) is a...This database helps identify gaps and duplicate studies in clinical research, facilitates clinical trial more
    University of Southern California (12/12/24)
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