Claudia Cabrera Varela
Louisville,KY
Summary
Professional with experience in clinical research coordination, equipped to make significant impact in this field. Demonstrated ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with results-driven approach that ensures successful study outcomes.
Overview
4
4
years of professional experience
Work History
Clinical Research Coordinator
Blue Ocean Medical Center
03.2023 - 01.2025
- Maintained knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedule tests, procedures, laboratory information, and drug accountability requirements.
- Recruited patients for studies, pre-qualify study participants.
- Resolved conflicts and addressed challenges within the team to maintain morale and productivity during high-pressure situations.
- Oversaw data collection and management processes to ensure accuracy and integrity of clinical trial data.
- Completed study documentation, including case report forms, study synopsis and other study specific documents.
- Coordinated and conduct patient care visits and assures all procedures are conducted in compliance with the clinical protocol.
Site Start Up and Regulatory Specialist
Spotlight Research
05.2021 - 03.2023
- Monitor basic financial aspects of the project and the number of hours/task available per contract
- Forecast submission/approval timeliness and ensures they are complied.
- Review Standard Operating Procedures (SOP)and work instructions in a timely manner and update training records accordingly.
- Optimized internal audit processes, identifying areas for improvement in regulatory adherence.
- Enhanced regulatory compliance by developing and implementing robust policies and procedures.
Education
Bachelor of Science - Biology
Florida International University
Miami, FL12-2019
Skills
- Strong skills in PC based documentation
- Superior presentation and communication skills
- Data collection techniques (Microsoft office)
- Good clinical practice
- Protocol development
- Site management
- Problem-solving abilities
Languages
English
Native or Bilingual
Spanish
Native or Bilingual
Timeline
Clinical Research Coordinator
Blue Ocean Medical Center
03.2023 - 01.2025
Site Start Up and Regulatory Specialist
Spotlight Research
05.2021 - 03.2023
Bachelor of Science - Biology
Florida International University
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