Graham Faught

Manager, Site & Patient Services at IQVIA
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Tampa Bay Area
Skills

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5.0

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Jalene Barnhart

Graham has excellent communication and problem-solving skills and was great to work with on a few previous clinical trials our site conducted. We hope to work with him again in the future.

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Credentials

  • Certified Pharmacy Technician (PTCB)
    -
    Jul, 2005
    - Nov, 2024

Experience

  • IQVIA
    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Manager, Site & Patient Services
      • Mar 2017 - Present

      • Manage employees in accordance with organizations policies & applicable laws. Responsibilities include planning, assigning, directing work; appraising performance & guiding professional development; rewarding & disciplining employees; addressing employee relations issues and resolving problems. Approve actions for all management / human resource matters• Participate in the selection and on-boarding process for new ISS employees by conducting candidate review and participating in the interview process. Ensure employees have the appropriate materials, systems access and training to complete job responsibilities• Manage the delivery of an accurate and robust patient and site operations plans in support of opportunities (including but not limited to Requests for Proposals).• Ensure Quintiles patient and site services is providing a competitive edge in winning new business.• Support patient and site operational plans at customer bid defense meetings and internal customers.• Obtain required information regarding future research plans, regional priorities, and capacity plans.• Maintain regular communication with staff in assigned therapeutic areas on non-project issues such as business strategy, mutual pipelines/planning performance trends across all studies (using performance scorecards) and compliance with contracts• Reconcile and interpret patient and site services data, providing solid recommendations and scenario planning as required. May provide site tiering /feasibility text for proposals and feasibility reports• Manage the generation, analysis and interpretation of study related information to produce and support recommendation of recruitment rates, country allocations and site tiering. May produce summary reports and present internally or externally.• Contribute to the process improvement through working with Quintiles processes to deliver quality and consistency• Serve as point of contact for issue escalation and process alignment

    • RWLPR Site Management Lead
      • Mar 2015 - Mar 2017

      Serves as Clinical Team Leader for a multi-operational project of multiple complexities. Provides clinical research expertise, site monitor leadership, and management of site clinical activities. Performs monitoring in compliance with FDA regulations and all related SOPs. Instructs the investigational site staff in their role and responsibilities in conducting clinical studies and evaluates site performance and compliance in conducting clinical studies. Monitors regulatory status of studies at sites. Responsible for the planning and delivery of the site management component of the project in accordance with the scope of work and contracted timeline. Development of project specific procedures/work instructions, project training for Site staff/investigators and SMSs. Provide CPMs necessary site management information as needed for the sponsor.

    • Senior Clinical Research Associate
      • Nov 2007 - Mar 2015

      Work on Phase I, Phase II and Phase III clinical studies as senior site monitor assuring compliance and site adherence to Good Clinical Practices and all FDA guidelines; working across several therapeutic areas (currently cardiovascular, ophthalmologic, gastrointestinal and vaccine) administer protocol-related training to sites and establishing regular communication with sites to create strong working relationships and promote subject recruitment/retention; knowledge of budget negotiations as well as contractual negotiations for potential clinical sites

  • Romark, L.C.
    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Clinical Research Associate
      • Aug 2005 - Aug 2007

      Worked on both Phase II and Phase III clinical studies as site monitor assuring protocol compliance, specialized in gastrointestinal diseases; worked hand-in-hand with regulatory affairs as regulatory specialist making sure all sites in compliance with FDA requirements; assured site adherence to Good Clinical Practices and all FDA guidelines; recruitment of applicable sites for both Phase II and Phase III clinical trials; knowledge of budget negotiations as well as contractual negotiations for potential clinical sites

  • Eckerd/CVS Pharmacy
    • Lead Pharmacy Technician
      • May 1999 - Aug 2005

      Lead technician in high volume store(500+ scripts per day); inventory specialist; daily interaction with customers in all facets of job; trained in all aspects of pharmacy; register trained; handle medications daily; data entry of prescriptions; new hire trainer in store; work hand in hand with all levels of the health care system; insurance specialist Lead technician in high volume store(500+ scripts per day); inventory specialist; daily interaction with customers in all facets of job; trained in all aspects of pharmacy; register trained; handle medications daily; data entry of prescriptions; new hire trainer in store; work hand in hand with all levels of the health care system; insurance specialist

Education

  • University of South Florida
    B.S., BioMedical Sciences
    2004 - 2008

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