FAQ About Angela Gatewood

• What is Angela Gatewood's address?

  Angela Gatewood is located at
  Memphis, Memphis, United States

• What is Angela Gatewood's job title?

  Angela Gatewood is a • Provide technical services for the collection, review, maintenance and tracking of regulatory documents from clinical sites • Track and ensure resolution of specific site discrepancies with data management • Track investigational site documentation ensuring receipt of proper study documentation, agreements, contracts, and Institutional Review Board approvals • Responsibilities include addressing study and site management and documentation issues of moderate complexity under direct supervision, utilizing analysis and judgment to effect solutions to meet goals and objectives • Coordinate in-house monitoring activities as related to the conduct of clinical trials • Generate and distributes agendas and minutes for protocol meetings • Initiate and prepare all site payments • Distribute and track clinical trial supplies , e.g. CRFs to ensure sites have sufficient supplies for recruitment • Review data in Electronic Data Capture system (EDC) • Consistently track and update trial information in the Clinical Trial Management System (CTMS) and electronic trial master file repository (RAD) • Manages study site activities and provide ongoing updates of site status to management • Ensure all study related communication including e-mail is tracked, printed and filed as required • Assist Clinical Trial Manager in the production of Status Reports. • Supported Senior Compliance Officer in a variety of complex regulatory and legal procedures • Coordinated day-to-day compliance activities including, but not limited to directing compliance questions based on current policies and procedures • Performed General Sanction Checks, e.g. OIG Sanction list • Prepared, maintained, and distributed compliance binders and training materials for Business Conduct Standards • Processed payments for quarterly consulting reports • Submitted appropriate consulting activity documentation to legal contract analyst for payment processing • Assisted with the database development and ongoing maintenance for consulting payments and other relevant activities • Scheduled appointments, meetings, conference rooms, and arrangements for briefings/depositions. • Coordinated in-house monitoring activities as related to the conduct of clinical trials • Provided technical services for the collection, review, maintenance and tracking of regulatory documents from clinical sites • Initiated follow-up with investigative sites in order to resolve any outstanding discrepancies • Participated in the entry of data into clinical administrative database for clinical projects (CTMS) • Performed administrative and clerical duties, as directed to include; filing, photocopying, ordering and maintaining supplies for regulatory document coordination • Generated and distributed agenda and minutes for protocol meetings • Initiated and prepared site payments • Tracked investigational site documentation ensuring receipt of proper study documentation, agreements, contracts, and Institutional Review Board approvals. • Tracked CRFs collected during monitoring visits to data management • Performed General Sanction Checks, e.g. OIG Sanction list • Reviewed Trip reports. • Assisted clinical staff to satisfy applicable regulatory standards and requirements for the conduct of clinical studies • Tracked investigational site documentation ensuring receipt of proper agreements, contracts, and Institutional Review Board approvals • Reviewed study documentation for completeness and accuracy and obtain corrections by working with internal and external resources, as applicable • Responsible for the retrieval and review of all clinical study data, review case report forms and radiographs for accuracy generate discrepancy resolution forms and review completed discrepancy documentation for accuracy • Prepared for site initiation visits, monitoring visits, and close-out visits, as applicable • Conducted periodic review of clinical study files for completeness • Provided administrative services supporting clinical staff such as filing, answering phones, copying, preparing shipping labels, preparing mass mailings, ordering office supplies, scheduling conference calls and meetings, and updating calendars • Organized and distributed clinical study documents and assist in the setup of filing and document management and tracking systems • Prepared site payments, maintain site payment summaries and develop site payment reports, as applicable. • Responsible for timely credentialing and re-credentialing of all physicians and ancillary medical providers associated within the organization • Responsible for development and planning credential process of medical staff physicians • Provided administrative and technical support to medical staff re-credentialing process as well as initial applications in accordance with policies and procedures; provide verification of reference documentation for physicians to include OIG sanctions, verification of licensure, medical insurance and education • Responsible for handling physician complaints regarding application status in relation to the approval or the renewal of current privileges as well as investigating any process delays in an effort to expedite the application process. • Assigned to Juvenile Court Division where I conducted detail search of child support cases through computerized system; managed the TCSE system and other computerized databases for case management • Resolved financial conflict within child support case system; prepared daily, weekly and monthly reports; prepare Excel documents for visualization of outstanding cases.• Created, managed and maintained slide presentations for all meetings • Acted as primary coordinator for the CACI demographic database used for strategic planning; responsible for GIS mapping used in strategic planning • Assisted with technical support for the installation process of various software • Trained employees on LCD equipment used for presentations • Worked with all levels of Senior Management in providing support for power point presentations.• Responsible for all office management to include patient charts, records, report and billing of Medicare expenditures; lead person over three (3) unit technicians • Managed time schedules for unit technicians • Assisted in evaluations completing personnel evaluations; managed inventory orders and reports; assisted in the assembly of dialysis equipment when needed • Acted as a liaison between the patient and their healthcare provider, by informing the healthcare provider of patient complaints that needed to be addressed upon the healthcare provider next visit to the unit.

• What industry does Angela Gatewood currently work in?

  Angela Gatewood currently works in the Medtronic |

• Which languages does Angela Gatewood speak?

  No Languages Available

• Which industries has Angela Gatewood previously worked in?

  Angela Gatewood has prior
  experience in the following industries:
  Methodist Healthcare | Shelby County Government

• What is Angela Gatewood’s work experience?

  Angela Gatewood has the following professional experience:
  Medtronic | Methodist Healthcare | Shelby County Government

• How can I find Angela Gatewood on LinkedIn?

  You can view Angela Gatewood’s LinkedIn profile at LinkedIn URL

• What are Angela Gatewood’s work email addresses?

  Angela Gatewood’s work email
  addresses are
  angela.gatewood@medtronic.com

• What company does Angela Gatewood work for?

  Medtronic |