Taryn Moore Email and Phone Number
Taryn Moore work email
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Taryn Moore personal email
Over 19 years of global clinical research experience, including 7 years of on-site monitoring and 12 years of study management. Extensive oncology background leading cross-functional teams at both the study and program levels, to plan and manage of all phases of clinical studies. Clinical research therapeutic areas/indications include:Hematology/ Oncology:Multiple MyelomaAdvanced Non-Hematologic MalignanciesHead and Neck CancerOvarian and Fallopian Tube CancerDiffuse Large B Cell LymphomaMetastatic Breast CancerAllergy/ Immunology:Allergic RhinitisInfluenzaRheumatology:Rheumatoid ArthritisGastrointestinal:Ulcerative ColitisInflammatory Bowel DiseaseCNS:Major Depressive DisorderBipolar DisorderCardiovascular:Acute Myocardial InfarctionHigh-Risk Cardiac Surgery with Cardiopulmonary BypassLipid LoweringOphthalmologyGlaucoma (Device)
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Global Trial ManagerJohnson & Johnson Innovative Medicine Aug 2022 - Present
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Project Director, Pra @ Jansenn Inc., Early Development OncologyPra Health Sciences Dec 2020 - Nov 2022Raleigh, North Carolina, Us -
Senior Clinical Project ManagerAthenex Oct 2017 - Dec 2020Buffalo, New York, UsResponsible for planning and management of clinical studies through the leadership of the cross-functional clinical study team. Oversees study level issue identification and resolution, and responsible for issue escalation to the program level. Works in collaboration with project leadership and multiple business-partners to facilitate communication with external partners and key therapeutic area investigators when issues arise that affect multiple projects and/or TA(s). Responsible for the development of study budgets, timelines and study plans including the monitoring plan, risk mitigation and escalation plan, safety management plan, data cleaning plan, and audit/QC visit plan. Provides expertise in managing sites and clinical monitoring activities utilizing advanced practices. Provides guidance for assessment, resolution, and documentation of both routine and complex site and study issues and ensure trial adherence to ICH/GCP/local regulations. Responsible for vendor management and adherence to study budgets and plans. Works with cross-functional departments to ensure timely and accurate projections for IP manufacturing, packaging, and IP shipments. Responsible for CSR planning and understanding requirements for IND/NDA submissions. -
Global Clinical Trial Manager/ Global Project ManagementDocs May 2016 - Sep 2017Leopardstown, Dublin, IeResponsible for planning and management of clinical studies conducted by Global Development through the leadership of the cross-functional clinical study team. Leading and continually reviewing risk mitigation activities to ensure study delivery to plan and contributing to study-level risk assessments. Responsible for reporting study progress at appropriate forums and to management. Collaborating with Regional CTMs to ensure country level study delivery aligned with global delivery plans. Oversee global insourcing/outsourcing partner deliverables to the required standards. Primarily responsible for managing study-level budget and timelines, partnering with Tech Services, Supplier Governance, and Electronic Trial Operations, to ensure vendor set-up, conduct, and quality oversight of deliverables. Leads global study-level documentation, development, and implementation of global Drug Supply Plan. Ensuring implementation of studies in accordance with SOPs and ICH/GCP guidelines -
Clinical Trial ManagerIcon Plc Jun 2015 - May 2016Dublin, IeAct as the Functional Lead from Clinical Research Services with responsibility for delivery of all clinical aspects of clinical studies. Oversee and serve as the liaison between the Project Manager and a group of Clinical Research Associates (CRAs) assigned to a given clinical study, for the delivery of all aspects of monitoring and site management, ensuring consistency with ICH/GCP and applicable ICON Standard Operating Procedures (SOPs), applicable regulations, the monitoring plan and ensuring the clinical portion of the study is inspection ready at all times. -
Clinical Trial ManagerClinipace Worldwide Nov 2013 - May 2015Morrisville, North Carolina, UsResponsible for the day to day leadership and management of monitoring services for clinical projects including direct communication and interaction with investigative sites/monitors/sponsors. Delivers monitoring services to Project Management. Serves as backup in the absence of Project Manager. Developed and maintained project specific tools and training materials. Review, managed and tracked trip reports. Provide sponsor support and communication for monitoring and the site which include conference calls, team training and meeting planning. Responsible for cohort management and slot assignments, including site correspondence to confirm slot availability and confirmation of assignments. Assist the Project Manager with coordination and management of the project budget, grant administration and sponsor invoicing. Prepare and deliver presentations to sponsors/industry. -
Clinical Research SpecialistQuintiles Sep 2011 - Oct 2013Durham, North Carolina, Us• Oversee the work of assigned CRAs, providing advice and guidance to help achieve quality deliverables on site. • Ensure that clinical monitoring tasks are conducted in accordance with protocol, process, quality standards, and expectations. • Responsible for cohort management and slot assignments, which includes site correspondence to confirm slot availability and assignments.• Identify quality issues within the study to implement appropriate corrective action plans. Escalate findings and action plans to appropriate parties.• Develop study management and clinical monitoring plans, training documentation for the study team, and guidance documentation for site staff.• Provide input and updates to the Clinical Project Manager regarding the monitoring status, progress, and deliverables. • Act as subject matter expert for operational conduct of the assigned protocol(s) at site.• Ensure that new project CRAs are brought on board and receive relevant study information. • Provide input to line managers on project team members’ performance relative to study tasks. • Prepare and present project information at internal and external meetings.• Ensure high performance and efficiency of the clinical team through the scheduling of co-monitoring/accompanied site visits and ongoing mentoring of CRA team. • Perform site visit report review -
Clinical Research Associate/ Sr. Clinical Research AssociateQuintiles Oct 2006 - Aug 2011Durham, North Carolina, Us
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Clinical Trials AssistantQuintiles Jan 2005 - Oct 2006Durham, North Carolina, Us
Taryn Moore Skills
Taryn Moore Education Details
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Buffalo State UniversityGeneral
Frequently Asked Questions about Taryn Moore
What company does Taryn Moore work for?
Taryn Moore works for Johnson & Johnson Innovative Medicine
What is Taryn Moore's role at the current company?
Taryn Moore's current role is Global Trial Manager, ED Oncology.
What is Taryn Moore's email address?
Taryn Moore's email address is ta****@****ahs.com
What schools did Taryn Moore attend?
Taryn Moore attended Buffalo State University.
What skills is Taryn Moore known for?
Taryn Moore has skills like Clinical Monitoring, Clinical Trials, Ctms, Clinical Research.
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