Deanna Glover - Clinical Research Coordinator Resume Simple
A clinical research coordinator with a strong background in the pharmaceutical industry. I have extensive experience in the medical field. I have worked in the areas of study and research as a clinical research coordinator.
Develops and implements recruitment strategies to ensure that the study is carried out the appropriate screening and enrollment process for each study.
Works with the Principal investigator to develop and implement the research project and the collection and analysis of data, including the development of the study, the planning, and implementation of the study.
Collaborates with the study Coordinator to design and implement recruitment strategies and contracts. Works with the Principal investigator to finalize the trial and submit to the IRB.
Assists with data collection and interpretation, writes and reviews reports, and provides recommendations for compensation. Coordinates and implements the study and/or staffing requirements.
Ensure compliance with protocol requirements, IRB and FDA regulations. Maintain accurate and complete records of all study activities.
Maintains and completes all required regulatory documents including but not limited to, but not limited to, IRB submissions, IND updates, continuing reviews, and annual renewals.
Performed analysis of the testing of the effects of the various species of the water. This included the development of the final report for the department.
Conducted literature reviews and presented findings at conferences and seminars. Wrote and edited grant proposals. Prepared and submitted grants.
Presented data to the National cancer Institute and the National Registry of health services. This included the development of a new research project for the department of public health.
Collected and analyzed data from the survey of the data. Presented the results at the annual conference. The project was published in the journal of the American Society of consultant.