• Frederick National Laboratory for Cancer Research (Bethesda, MD)
    …research, CMRPD services include comprehensive clinical trials monitoring, regulatory , pharmacovigilance, protocol navigation and development, and programmatic and ... Research's (CCR) Office of the Clinical Director for protocol development review, regulatory review, and the implementation process as well as oversees medical… more
    Neuvoo (12/02/19)
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  • Aerotek (Sacramento, CA)
    …Obtain city certifications for IRB Site initiation visits- the assigned regulatory coordinator would have to attend this. Submissions are done via IRB-Net ... Affairs Coordinator for Clinical Trials in Oncology: The Regulatory Coordinator will work with regulatory files and relevant communications must… more
    Neuvoo (12/09/19)
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  • Aerotek (Sacramento, CA)
    …city certifications for IRBSite initiation visits- the assigned regulatory coordinator would have to attend this. Submissions are done via IRB-NetThe ... Affairs Coordinator for Clinical Trials in Oncology: The Regulatory Coordinator will work with regulatory files and relevant communications must… more
    PandaLogic (12/07/19)
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  • Novo Nordisk (NJ)
    …well as the submissions published and processed by the Regulatory Operations Publishing Coordinator Processes electronic files incorporating bookmarks, links ... e- submissions and use of Insight Publisher and/or novoDOCS for regulatory submissions in NNI. RelationshipsThis person will report to the Director … more
    Healthjobsnationwide (12/10/19)
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  • Regeneron Pharmaceuticals, Inc. (Rensselaer, NY)
    …ex-US commercial filings completed by partners o Creates/maintains content trackers for regulatory submissions for assigned programs o Keeps management and ... supporting the deliverables and continuous improvement projects of the CMC Regulatory Sciences department to ensure timelines are met, potential resource constraints… more
    Neuvoo (12/02/19)
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  • Merck (Boston, MA)
    …sourcing of nonclinical safety studies (GLP and non-GLP) for inclusion in regulatory submissions . Interact directly with external client service representatives ... Safety Assessment and Laboratory Animal Resources (SALAR) is looking for a Sourcing Coordinator to help support the contracting of nonclinical studies. The Sourcing … more
    Healthjobsnationwide (12/11/19)
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  • NPAworldwide Recruitment Network (Palm Harbor, FL)
    JOB DESCRIPTION Job #: 28483 Title: Regulatory Affairs Coordinator , Medical Devices, Palm Harbor, FL Job Location: Palm Harbor, Florida - United States ... NO WHY IS THIS A GREAT OPPORTUNITY? As the Regulatory Affairs Coordinator YOU will be part...by business objectives. Prepare in-country specific documentation to support submissions and monitor reports and responses to regulatory more
    NationJob (12/10/19)
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  • Hogan Lovells (Washington, DC)
    …Business Development (M&BD) team is seeking the right candidate to serve as aM&BD Coordinator for our Energy and Environment regulatory practices and our Energy ... and Natural Resources (ENRG) industry sector group. The M&BD Coordinator will be part of a global team working collaboratively to ensure that objectives and plans… more
    Neuvoo (12/12/19)
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  • Imagine Staffing Technology (Rochester, NY)
    IMAGINE STAFFING is recruiting for a seasoned Clinical Trials Coordinator for a Rochester, NY based client. The Coordinator will manage and oversee the Clinical ... feasibility. Reviews the feasibility assessment form that accompanies protocol submissions . Prepares agenda items and disseminates information to board members.… more
    Neuvoo (12/09/19)
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  • American Cybersystems, Inc. (ACS Group) (Plainsboro, NJ)
    …well as the submissions published and processed by the Regulatory Operations Publishing Coordinator Processes electronic files incorporating bookmarks, links ... of e- submissions and use of Insight Publisher and/or novoDOCS for regulatory submissions in NNI. Relationships This person will report to the Director … more
    Neuvoo (12/05/19)
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  • ApotheCom: A MEDiSTRAVA Company (Medical Division… (PA)
    Project Coordinator Position Profile Part of the ApotheCom Client Services team, the Project Coordinator provides comprehensive team, administrative, and project ... that projects and services consistently meet client needs. The Project Coordinator interacts with internal departments including Scientific, Creative, and Finance to… more
    Neuvoo (12/12/19)
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  • Phenomix Sciences (St. Cloud, MN)
    …Phenomix Sciences is seeking a dynamic, successful, action-oriented Clinical Research Coordinator to support pilots and/or trials related to the products currently ... feasibility and develops new trial protocols Creates and manages grant submissions and protocol documents including, editing, amending, proofing Prepares documents… more
    Neuvoo (12/09/19)
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  • Indiana University (Indianapolis, IN)
    …in Pulmonary Medicine. Assist with protocol development, study feasibility, IRB submissions and maintaining regulatory compliance. Recruit subjects and oversee ... Job Summary The primary role of the Clinical Research Coordinator is to initiate and coordinate clinical research studies...design and risk to target population. Compose and prepare regulatory / IRB documents for new study submissions ,… more
    Neuvoo (12/09/19)
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  • Digestive Health Research (Nashville, TN)
    The Clinical Research Coordinator II (CRC II) assists the applicable research operations leadership, supervisors or Site Directors, and Investigators in the ... fashion. Supervise site initiation activities, including creating and submitting all Regulatory and site-specific documents, oversight during site start-up, interim … more
    Neuvoo (12/09/19)
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  • Medix (TM) (Denver, CO)
    …reconciliation, lab data reconciliation and safety coding * May be responsible for regulatory submissions . Need working knowledge of essential documents and IRB ... Clinical Research Coordinator Position Summary: The candidate will be coordinating...Good Clinical Practices. Responsibilities * May be the sole coordinator or work in collaboration with a research nurse… more
    Neuvoo (12/12/19)
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  • Indiana University (Indianapolis, IN)
    …screening of study subjects; act as a liaison with sponsors, collaborators and regulatory agencies. The incumbent will perform varied routine and non-routine task of ... (ie informed consent, protocol and protocol summary). Maintain current knowledge of regulatory affairs and/or issues. * Review and assess each clinical research… more
    Neuvoo (12/09/19)
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  • Kelly Scientific Resources (North Chicago, IL)
    …compliant with all current industry requirements as they relate to regulatory submissions , including electronic submission/approval standards. Participates in ... Seeking a Medical Writing Word Processing Coordinator I for a 3 month assignment in...Clinical Study Reports, Investigators Brochures, and other related clinical regulatory documents. Provides document formatting support to Medical Writing,… more
    Neuvoo (12/04/19)
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  • A-Line Staffing Solutions (Waukegan, IL)
    …compliant with all current industry requirements as they relate to regulatory submissions , including electronic submission/approval standards. Participates in ... Full time Medical Writing Processing Coordinator in Waukegan, IL area with a major...Clinical Study Reports, Investigator's Brochures, and other related clinical regulatory documents. Provides document formatting support to Medical Writing,… more
    Neuvoo (12/04/19)
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  • Ascent (South San Francisco, CA)
    …investigational sites to meet enrollment goals and timelines Presents at Investigator/Study Coordinator meetings, as needed Work with IRB submissions Mandatory: ... Coordinator lll South San Francisco 1 Year Contract...other study-related documents using knowledge of GCP/ICH and other regulatory requirements Assists study manager with the investigator contract,… more
    Neuvoo (12/09/19)
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  • AbbVie (Mettawa, IL)
    …compliant with all current industry requirements as they relate to regulatory submissions , including electronic submission/approval standards. Responsible for ... and electronic QC) associated with electronic document-related activities for regulatory documents. Communicates deliverables, electronic document process, and durations… more
    Neuvoo (12/02/19)
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