Experienced and reliable research professional with over 10 years of experience in the pharmaceutical industry. Strong background in molecular biology and biochemistry. Proficient in Microsoft office, MS Excel, MS PowerPoint, and Adobe.
Project Manager for the company of the patient. Responsibilities included: The management of the lab, and the preparation of the reports.
Performed supervisor of the lab and assisted in the preparation of scientific papers. Assisted in the development of a new animal model.
Assisted in the preparation of manuscripts for publication. Presented findings at conferences and seminars. Participated in the development of a new research study.
Maintained accurate records of patient visits, adverse events, and serious adverse events. Maintained study files and records.
Performed data entry, source document verification, and other study related activities. Assisted in the preparation of reports for submission to sponsors.
Performed data analysis and analyzed results for the research project. Assisted in the development of a new database for the research and development of the study.