Sabrina L.

Key Skills

Software

Other

Top Subject Matter

Clinical research / Bioinformatics / Regulatory documentation

Clinical research administration / participant scheduling / study documentation

Legal Services & Contract Review

Top Data Types

Document

Text

Top Task Types

Classification

Data Collection

Freelancer Overview

Bioinformatics Intern (Data organization, validation, and documentation) — University of California, San Diego. Brings 3+ years of professional experience across legal operations, contract review, compliance, and structured analysis. Core strengths include Other. Education includes Bachelor of Arts, University of California, Santa Cruz (2022). AI-training focus includes data types such as Document and labeling workflows including Classification and Data Collection.

Labeling Experience

Bioinformatics Intern (Data organization, validation, and documentation) — University of California, San Diego

OtherDocumentClassification

Managed and organized clinical and research datasets by ensuring records were complete, properly structured, and aligned with established protocols. Performed data entry, validation, and reporting using regulated systems and documentation workflows to support accurate study deliverables. Corrected identified data issues and implemented best-practice documentation to maintain institutional and regulatory compliance. • Prepared and maintained clinical data, survey data, specimen logs, and regulatory documentation • Built standardized templates and data workflows to improve consistency and usability • Conducted error identification and corrections to improve dataset reliability • Used Excel and regulated platforms to support data entry, validation, and reporting

2024 - 2024

Clinical Research Coordinator (Maintain study records and schedule documentation) — University of California, San Francisco

OtherDocumentData Collection

Coordinated clinical research study administration while maintaining accurate study documentation and participant records using electronic systems. Performed ongoing creation and maintenance of visit schedules, participant itineraries, and study records to support regulatory compliance and timely milestones. Conducted regular audits and corrections of study records to ensure alignment with IRB and FDA standards. • Created and maintained detailed visit schedules and participant itineraries • Managed study records and documentation for multiple concurrent research studies • Conducted audits and corrections to ensure record accuracy • Coordinated communications and documentation between investigators and research staff

2022 - 2024

Education

Work History