Amanda Baldwin - Program Manager Resume Simple
A highly motivated and detail-oriented professional with over 15 years of experience in the healthcare industry. Strong background in customer service, and management.
  • management, office, teaching, epic, microsoft, mentoring, microsoft office, research, laboratory skills, project management, laboratory, clinical
  • rna, dna, data acquisition, recruitment, laboratory, clinical, research, implementation, clinical trial
  • 2017-12-252017-12-25

    Program Manager

    Cigna Corporation

    • Clinical research Coordinator: Supervise and train new employees, and oversee the day-to-day operation of the laboratory.
    • Provide ongoing management and support for research projects including but not limited to: Briefing and review of data, preparation of reports, and other related documents.
    • Provide technical support to research and development staff in the use of the research project and the coordination of the study.
    • Provides technical support to research and development staff in the use of the research project. Identifies and documents data for the study.
    • Provide assistance to research projects in the development of the research project. The use of Microsoft office applications, such as the data management system (LIMS).
    • Perform research and development experiments for the purpose of monitoring and mentoring of research assistants. Conduct and train new lab personnel.
  • 2017-12-252017-12-25

    Program Coordinator

    Samsung Electronics America

    • Assisting in the development and implementation of clinical trials, including recruitment, protocol, and data collection, and database lock.
    • Coordinated with the laboratory Director of pathology and lab to develop and implement protocols for the collection of DNA and RNA samples.
    • Conducted research studies on the development of a new method for the detection of human blood and urine. Also, performed the evaluation of the data collected.
    • Managed study start-up activities, including data review, query resolution, and trial close-out. Reviewed and resolved queries.
    • Assisted in the preparation of study protocols, amendments, and regulatory documents for trial Master file. Responsible for the review of investigator files and protocol deviations.
    • Managed and maintained databases for study protocols, case report forms, and data analysis. Performed and documented study visits and procedures.


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