• RHOAR Phase I/Program Coordinator

    Cumberland River Behavioral Health, Inc. (Middlesboro, KY)
    Job Title: Phase I/Program Coordinator Summary of Job Duties: The Phase I/Program Coordinator is responsible for coordinating, planning, and implementing the ... program content of Phase I. Supervises the Motivational Track Coordinator, Assistant staff...client's progress (or lack of) while in program. f. Monitor the general health of clients, and refer to… more
    Cumberland River Behavioral Health, Inc. (09/19/24)
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  • Clinical Research Monitor I

    University of Colorado (Aurora, CO)
    ** Clinical Research Monitor I** **Description** **University of Colorado Anschutz Medical Campus** **Department: Clinical Research Support Team (CReST)** ... **Job Title: Clinical Research Monitor I** **Position #: 827305 - Requisition #: 34812**...investigator-initiated research. + Three or more years of interventional clinical research experience, Including experience with Phase more
    University of Colorado (09/08/24)
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  • Senior Director Global Regulatory Leads (Early…

    Lilly (Indianapolis, IN)
    …as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency ... Initiate andmaintainregulatorystrategydocuments byleveragingteam expertise, as well as scientific, drug/device clinical development and knowledgefromhealth authorities such as regulatory policies,… more
    Lilly (08/24/24)
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  • Clinical Trial Research Monitor

    Pennsylvania State University (Hershey, PA)
    …at the Penn State College of Medicine, Hershey, PA, is hiring a full-time Clinical Trial Research Monitor . The Beat Childhood Cancer Research Consortium (BCC) is ... Beat Childhood Cancer (beatcc.org) (https://research.beatcc.org/) Job Duties & Responsibilities: The Clinical Trial Research Monitor is primarily responsible for… more
    Pennsylvania State University (08/23/24)
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  • Early Development Clinical Research…

    Lilly (IN)
    …Responsibilities** The primary responsibilities of the CRP are generally related to early phase clinical studies and late phase biopharmaceutical submission ... experience, or similar, that provides adequate background relevant to clinical trial design and conduct of Phase ...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
    Lilly (11/01/24)
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  • Clinical Research Coordinator A/B/C…

    University of Pennsylvania (Philadelphia, PA)
    …supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, ... of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to...patient visits and any necessary testing. Conduct patient visits. Monitor patients per protocol requirements and ensure adherence to… more
    University of Pennsylvania (10/27/24)
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  • Senior Associate Central Monitor , Risk…

    Pfizer (Groton, CT)
    …experience in the clinical development fields. + Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of ... contribution will directly impact patients. **What You Will Achieve** The Sr. Central Monitor is responsible for ensuring the completeness, quality and integrity of … more
    Pfizer (11/07/24)
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  • VP, Clinical Development

    Taiho Oncology (Princeton, NJ)
    VP, Clinical Development Princeton, NJ, USA Req #306 Friday, August 16, 2024 Looking for a chance to make a meaningful difference in the oncology space? Taiho ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
    Taiho Oncology (08/17/24)
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  • Early Development Clinical Research…

    Lilly (Indianapolis, IN)
    …of the Early Development Clinical Research Physician are generally related to clinical pharmacology including early phase exploratory and late phase ... etc. + Contribute, as an integral member of the Clinical Pharmacology team, to global Phase I...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
    Lilly (10/31/24)
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  • Director, Clinical Science, ENHERTU

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …and/or adjudication committee setup; Interacts with KOLs and PIs to plan study and monitor completion + Study outputs: For Phase 2 studies: Drafts responses to ... (CSL) or major scientific/medical contributor; For large or complex Phase 2 studies: Provides the strategic direction to BD&O...valid clinical interpretation of study results as Clinical Study Leader, medical monitor or regional… more
    Daiichi Sankyo Inc. (10/24/24)
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  • Clinical Research Coordinator 2 (Gastro…

    Stanford University (Stanford, CA)
    Clinical Research Coordinator 2 (Gastro Studies) **School of Medicine, Stanford, California, United States** Research Post Date Aug 29, 2024 Requisition # 104444 ... major contributions in basic research, a new commitment to clinical and outcomes research, a track record of training...disease, alcohol-associated liver disease, and cirrhosis, and will include Phase 1, Phase 2, and Phase more
    Stanford University (08/30/24)
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  • Coordinator, Clinical Studies…

    MD Anderson Cancer Center (Houston, TX)
    …Also serves as an effective point of contact regarding status and progress of phase I trials. Impacts clinical trials patients in designated protocols. Utilizes ... educational, emotional, and psychosocial needs of patient and their families while on phase I clinical trials. . Coordinate, evaluate, and follow the patient's… more
    MD Anderson Cancer Center (10/24/24)
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  • Medical Director - Early Clinical

    Amgen (Washington, DC)
    …is looking for a Medical Director. The Medical Director will lead early phase clinical development of oncology compounds from first-in-human studies through ... proof of concept. They define, design, and implement early phase clinical and translational projects as the...an internal clinical expert in translational and clinical oncology. + Serve as medical monitor more
    Amgen (10/07/24)
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  • Monitor Technician

    Trinity Health (Syracuse, NY)
    …monitors or EKGs is strongly preferred.** + Successfully completes Phase 1 and Phase 2 of the Monitor Technician orientation program or the equivalent. + ... availability to train full time for 4 weeks.** **WORK ENVIRONMENT AND HAZARDS:** Clinical setting. Exposure class I - -Routine or potential exposure to blood, body… more
    Trinity Health (09/21/24)
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  • Clinical Research Associate III-Senior

    WuXi AppTec (Austin, TX)
    …and within budget. The Senior CRA will work to manage, oversee and may monitor /co- monitor clinical trial sites. **Essential Job Functions:** + Participate in ... Organization (CRO) providing a comprehensive range of services in clinical development. We provide Phase I to...project needs + Approximately 50% to study sites to monitor , co- monitor , train, attend Investigator meetings or… more
    WuXi AppTec (10/14/24)
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  • Clinical Research Coordinator B/C…

    University of Pennsylvania (Philadelphia, PA)
    Clinical Research Coordinator B Job Description Summary With minimal supervision: the clinical research coordinator will coordinate Phase I-IV clinical ... of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to...patient visits and any necessary testing. Conduct patient visits. Monitor patients per protocol requirements and ensure adherence to… more
    University of Pennsylvania (10/27/24)
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  • Clinical Research Nurse

    Actalent (Kokomo, IN)
    …Responsibilities + Support and manage oncology clinical trials, primarily in Phase 2-3. + Administer chemotherapy and monitor patient responses. + Assist ... Job Title: Clinical Research Nurse Job Description We are seeking...successful candidate will support current oncology trials, primarily in Phase 2-3, and assist with an RO1 grant related… more
    Actalent (11/05/24)
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  • Clinical Research Project Manager A/B…

    University of Pennsylvania (Philadelphia, PA)
    …(ie, multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I - IV clinical trials and registries within the ... concert with investigators, detailed documentation of study activities). + Monitor subjects per protocol requirements and ensure adherence to...budget preparation for trials as needed. May support a clinical trial budget through each phase of… more
    University of Pennsylvania (11/01/24)
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  • Clinical Research Coordinator B/C (Hybrid…

    University of Pennsylvania (Philadelphia, PA)
    …(ie multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I - IV clinical trials and registries within the ... concert with investigators, detailed documentation of study activities). + Monitor subjects per protocol requirements and ensure adherence to...budget preparation for trials as needed. May support a clinical trial budget through each phase of… more
    University of Pennsylvania (10/28/24)
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  • Sr. Clinical Trial Project Manager (Center…

    University of Pennsylvania (Philadelphia, PA)
    …the development of new treatments and the translation of this research into early phase clinical trials. Job Description The Sr. Clinical Trials Project ... the Sr Clinical Trial Project Manager will independently manage a portfolio of Phase I Penn-Sponsored clinical research studies. The Sr. Clinical Project… more
    University of Pennsylvania (10/27/24)
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