Katherine Lopez Boza

04.2021 - Current

Prepared documents, reports, and presentations detailing results and conclusions.
Reviewed literature extensively to stay informed about industry trends and advancements in related fields of study.
Managed multiple projects simultaneously, ensuring timely completion and high-quality results.
Increased research efficiency by streamlining data collection and management processes.
Organized regular training sessions for team members on various topics such as statistical software usage or research ethics protocols.
Implemented new data analysis techniques to improve accuracy of research outcomes.
Improved participant recruitment strategies, leading to a higher number of qualified candidates for studies.
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Followed informed consent processes and maintained records.
Monitored patient safety throughout clinical trials and reported any adverse events.
Maintained compliance with protocols covering patient care and clinical trial operations.
Managed patient recruitment, informed consent process and data entry to support trial objectives.
Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
Prepared and maintained regulatory documents for clinical trial submissions.

Summary