• Amerantbank (Miramar, FL)
    …during internal/external audits or regulatory examinations.Assist the BSA High Risk Customer Manager and BSA High Risk Customer Team Lead during regulatory exams, ... special law enforcement requests, and/or special projects as necessary.Able to carry out to completion of high risk account reviews with minimal supervision.Able to produce top quality investigative cases that can be held to high standards of quality and… more
    JobGet (06/09/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionPosition Description: Senior Study Manager - Cardiometabolic Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare ... management deliverables, protocol level plans/timelines, country/site selection, system updates, Investigator Meeting planning, communication plans, preparation of status update… more
    HireLifeScience (06/05/24)
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  • Merck & Co. (Rahway, NJ)
    …and adverse event reporting-requirements internally and externally.The CRM (Clinical Research Manager ) could be responsible for a particular study for several ... performance issues and training-needs to CRA (Clinical Research Associate) manager and/or functional vendor and internal management as-needed.Performs Quality… more
    HireLifeScience (06/07/24)
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  • Northeast Georgia Health System, Inc (Gainesville, GA)
    …Complete status reports and communicate with the sponsor, research staff, Research Manager and Investigator (s). Update central progress tracker.Work with the key ... for subject enrollment and compliance from entry through follow up, investigator participation, data report submission and audits.Responsible for management of… more
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  • Eisai, Inc (Nutley, NJ)
    …coding practices among International offices.Interface with Clinical for investigator training Essential Functions Adverse event information collection, processing, ... professionals and consumers regarding post-market adverse experiences, and clinical investigators and their staff regarding AE's from clinical trials. 30%Assist… more
    HireLifeScience (05/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …support to uphold the ethical conduct of interventional, non-interventional, investigator -initiated trials, Managed Access programs and Collaborative Research to the ... support to uphold the ethical conduct of interventional, non-interventional, investigator -initiated trials, Managed Access programs and Collaborative Research to the… more
    HireLifeScience (06/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders.Summary The Manager of Data Governance Stewardship will work in areas required for the ... Signatures o 21 CFR 312.32: IND Safety Reports o FDA Guidance for Clinical Investigators , Sponsors, and IRBs - Adverse Event Reporting to IRBs - Improving Human… more
    HireLifeScience (04/12/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and International Conference on Harmonization (ICH) guidelines.The Senior Clinical Study Manager will have routine interaction with key internal and external ... abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a tactical study delivery role, reporting… more
    HireLifeScience (05/22/24)
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  • Merck & Co. (North Wales, PA)
    …studies to internal and external stakeholders such as outside Investigators /Suppliers and Key Opinion Leaders.Coordinate confidentiality, consultant agreements and ... external engagement meetings.Participate in quality control and integrity of study data and reports for publications.Manage publication development including formatting, figure/data content development, co-author review, internal review process, and journal… more
    HireLifeScience (06/06/24)
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  • Aequor (Thousand Oaks, CA)
    Remote Copy of AMAGJP00012547 Scrubbed resume attached Regulatory Writing Senior Manager ln this vital role role you will serve as the functional area lead on ... of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed… more
    HireLifeScience (06/08/24)
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  • Eisai, Inc (NJ)
    …is your profile, we want to hear from you. Job Summary The Senior Manager , Medical Writing will be the designated Lead Medical Writer for approximately 3-4 Programs. ... clinical sections of submissions documents such as briefing books, Global Investigator Brochures (GIB) and annual regulatory reportsPrepare and review marketing… more
    HireLifeScience (05/28/24)
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  • Merck & Co. (North Wales, PA)
    …trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update ... reports, study close out activities).Leads team for timeline management, risk identification and mitigation, issue resolution.May facilitate and collaborate with key internal/external stakeholders (eg, study team, country teams, vendors, committees) in support… more
    HireLifeScience (06/07/24)
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  • Bering Straits Native Corporation (Beavercreek, OH)
    …of Bering Straits Native Corporation, is currently seeking a qualified Program Manager supporting blockchain analysis in Baltic States. The ideal Program Manager ... development, custody of evidence, and asset forfeiture. The ideal Program Manager will bring project/program management experience with cybercrime; crime using… more
    JobGet (06/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence ... archive. Bring issues with the reconciliation to the attention of the Study Manager and propose remediation plan.Distribute key study documents to the CRO and… more
    HireLifeScience (06/06/24)
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  • Northeast Georgia Health System, Inc (Gainesville, GA)
    …etc. Complete status reports and communicate with the sponsor, research staff, Research Manager and Investigator (s). Work with the key functional departments to ... subject enrollment and compliance from entry through follow up, investigator participation, data report submission and audits. Minimum Job QualificationsLicensure… more
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  • Merck & Co. (Rahway, NJ)
    …assigned protocols and sites in a-country.-Under the oversight of the CRA manager the person ensures compliance of study conduct with-ICH/GCP and country ... requirements internally and externally.Acts as primary site contact and site manager throughout all phases of a clinical research study,-taking overall… more
    HireLifeScience (06/05/24)
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  • Bering Straits Native Corporation (Morgantown, WV)
    …mentioned above that have been coordinated with the COR and the Program Manager . Receive, receipt for, and safely transport serum samples and specimens (DASH) to ... have been coordinated with the COR and the Program Manager . Receive, receipt for, and safely transport serum samples...of the United States.Have not had a previous private investigator or security guard license revoked or denied in… more
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  • Bering Straits Native Corporation (Durham, NC)
    …mentioned above that have been coordinated with the COR and the Program Manager . Receive, receipt for, and safely transport serum samples and specimens (DASH) to ... States.Meets all basic qualificationsHave not had a previous private investigator or security guard license revoked or denied in...regular testing. Details to be provided by the hiring manager . Employees are expected to comply with all current… more
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  • Bering Straits Native Corporation (Cincinnati, OH)
    …above that have been coordinated with the COR and the Program Manager . Conduct visitor center operations that include issuing badges; maintaining visitor records; ... of the United States.Have not had a previous private investigator or security guard license revoked or denied in...law enforcement official, or a person licensed as an investigator or guard;Made any false report with respect to… more
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  • BioAgilytix (Boston, MA)
    …to review by the project manager (eg, Bioanalytical Project Manager (BPM), Principal Investigator )independently creating reports, plans, and submission ... documents in support of internal BioAgilytix projects Extracts and formats data from multiple lab systems (eg, LIMs, SoftMax, FACs) to generate reportsEssential Responsibilities: System FacilitatorSupport system implementation and updates, such as Watson LIMS… more
    HireLifeScience (05/03/24)
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