Director of Operations
Senior Vice President
Chief Financial Officer
Chief Operating Officer
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
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.
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.