Katherine Lopez Boza
Miami,FL
Summary
Detail-oriented Research Coordinator familiar with documentation, reporting and compliance guidelines. Specializing in study design and protocol development. Prepared to leverage expertise and 3 years of experience to make an immediate positive impact on research management at Lenus Research & Medical Group, LLC. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
Overview
3
3
years of professional experience
Work History
Research Coordinator
Lenus Research & Medical Group, LLC
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.
Education
Associate of Nursing - Nursing
EDP University of Puerto Rico
Hato Rey, PR08.2023
Skills
- Data organization
- Data Collection
- Project Management
- Research design
- Ethics compliance
- Participant screening
- Study protocols
- Informed consent
- Protocol development
- Research experience
- Patient recruitment
- Data collection techniques
- Trial management
- Good Clinical Practices
- Medication Dispensing
- Documentation requirements
Languages
Spanish
Native or Bilingual
English
Native or Bilingual
Timeline
Research Coordinator
04.2021 - Current
Associate of Nursing - Nursing
EDP University of Puerto Rico