Shakirat Akinde

Clinical Data Abstractor - Laboratory Corporation of America

(2021-11)

Reviewed and abstracted clinical information from electronic medical records according to registry and project guidelines.
Ensured accuracy, completeness, and consistency of patient data submitted to clinical databases.
Identified documentation discrepancies and collaborated with healthcare providers for clarification.
Performed quality audits to maintain high levels of data integrity.
Maintained compliance with HIPAA and organizational confidentiality policies.
Analyzed data to optimize business operations, communicating insights through data visualizations and detailed reports to support decision-making.
Reviewed data reports and performance indicators, identifying and correcting code discrepancies to ensure data accuracy.
Compiled reports highlighting trends, patterns, and predictions to inform management decisions using relevant data.
Used statistical tools to identify, analyze, and interpret patterns and trends in complex data sets.
Worked closely with business stakeholders in collecting data, performing analyses, creating visualizations, & presenting actionable data-driven insights.

Clinical Research Associate - Laboratory Corporation of America

(2013-12 - 2021-11)

Developed study procedures, methodology, and instructions for clinical trial staff, as well as designed data collection tools (case report forms).
Developed study procedures and instructions for clinical trial staff. Designed data collection tools, including case report forms.
Ensured compliance with good clinical practices and federal regulations for clinical investigations through in-depth knowledge of guidance documents and human subject protection.
Conducted chart reviews, observed research protocols, administered study medications, and managed regulatory paperwork including IRB submissions and renewals per FDA, IRB, and hospital guidelines.
Promoted good clinical practice in the conduct of clinical investigations by possessing in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection.
Reviewed information from clinical trials to ensure the accuracy of data gathered.
Collected, verified, and finalized data to create comprehensive reports and present findings to medical staff.
Analyzed healthcare data to optimize business operations and communicated results with data visualization and detailed reports.
Tested and implemented study databases. Supported clinical trials for CRO by providing meticulous data management.

Project Manager (Cancer - Cytogenetics Department) - Baylor College of Medicine

(2012-05 - 2013-12)

Organized laboratory workflows to meet timelines for clinical trials and diagnostic testing, including FISH and SNP array analysis, ensuring efficient sample processing.
Communicated between laboratory staff, physicians, and genetic counselors regarding specimen status and test results.
Tracked project timelines and maintained quality records while managing supplies and coordinating with genetic counselors and physicians for seamless operations.
Assisted in the interpretation of case results, and compiled completed case data for review.
Reviewed test forms for accuracy and reported any discrepancies.
Ensured that customer expectations were documented and acted upon in compliance with regulatory requirements.
Managed laboratory inventory, schedules, and administrative documentation.
Participated in activities designed to improve customer satisfaction and business performance.
Engaged in initiatives to enhance customer satisfaction through feedback collection and analysis.

About