Thomas Redman - Senior Manager Resume Simple
SUMMARY
A highly motivated, detail-oriented, and results-driven professional with over 15 years of experience in the pharmaceutical industry. Strong background in the areas of pharmacy and medical device industries.
SKILLS
  • audits, assessment, evaluations, responsible, drug safety, safety, fda, writing
  • management, neurology, therapeutic, budget, responsible, infectious disease, cardiovascular, oncology
WORK EXPERIENCES
  • 2017-12-252017-12-25

    Senior Manager

    Kroger

    • Assisted in the development and implementation of the FDA and other regulatory documentation for the research studies. Provided training and mentoring to junior CRAs.
    • Provide training and supervision for all aspects of the safety assessment and the preparation of the final report for the FDA.
    • Manage the development and monitoring of annual and annual performance evaluations, including the development of new hire training programs, and the planning of the program.
    • Assists in writing and reviewing of internal audits and annual reports for the FDA. Reviews and approve all regulatory documents.
    • Responsible for the development and execution of the company's policies and procedures. Support the development of the project and the business plan.
    • Provides technical support to the development and commercialization of new products and processes. Develop and implement the product and process improvement strategy.
  • 2017-12-252017-12-25

    Clinical Project Manager

    Career Connect Live

    • Member of the project management team responsible for the development and execution of the budget and operational plans. Developed and implemented a new study for the company.
    • Worked with cardiovascular, Neurology, oncology, and pediatric trials to develop and implement strategies for the development of new protocols and procedures.
    • Supported the development of therapeutic and medical Affairs for the EU affiliates. Developed and implemented a new study for the Bayer global Oncology group.
    • Reviewed and verified data for Phase III trials in infectious disease and infectious disease. Conducted site visits for sites.
    • Reviewed and approved study specific documents for completeness and accuracy. Developed and implemented corrective action plans. Identified and resolved issues.
    • Reviewed and approved study specific documents for completeness and accuracy. Developed and implemented corrective action plans. Ensured that all study deliverables are met.