Summary
Overview
Work History
Education
Skills
Software
Timeline
Generic

Aisha Tabor

Clinical Research Associate
Detroit,MI

Summary

Competent clinical research associate skilled at conducting site visits to check clinical operations and correct participant, documentation, or procedure issues. Diligent in performing studies aligned with good clinical practices, study-specific requirements and clinical monitoring plans. Excellent attention to detail with organizational and prioritization skills for efficient productivity. Supports participant recruitment and management to meet research objectives.

Overview

2
2
years of professional experience
11
11
years of post-secondary education

Work History

Clinical Research Associate

Henry Ford Health
09.2022 - Current
  • Optimized patient retention rates by establishing rapport with participants and addressing their concerns promptly.
  • Identified areas for process improvement within clinical trials, implementing changes to enhance overall project efficiency and quality.
  • Monitored safety of human subjects and oversaw consent procedures to comply with local and federal regulations.
  • Developed strong relationships with investigators and site personnel to ensure ongoing compliance with study requirements.
  • Maintained awareness of industry trends by attending conferences and participating in relevant professional development opportunities.
  • Enhanced data quality by closely monitoring study progress and ensuring accurate data collection.
  • Collaborated with cross-functional teams to successfully meet project timelines and deliverables.
  • Maintained comprehensive knowledge of applicable regulations and guidelines, ensuring full compliance throughout all stages of clinical trials.
  • Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
  • Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
  • Conducted clinical trial in accordance with protocol and recorded and monitored progress.
  • Liaised with clinical project leader to effectively resolve study-related issues.
  • Interfaced with clinical investigators and site staff to foster ethical research consistent with research plans.
  • Monitored patient safety throughout clinical trials and reported any adverse events.
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
  • Managed patient recruitment, informed consent process and data entry to support trial objectives.
  • Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Gathered lab specimens.
  • Followed informed consent processes and maintained records.
  • Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.

Clinical Assistant

Michigan Spine And Brain Surgeons
06.2022 - 10.2022
  • Reduced wait times for patients by efficiently managing check-ins, insurance verification, and payment processing.
  • Improved patient satisfaction by handling queries and concerns with empathy and professionalism.
  • Coordinated referrals from primary care physicians to specialists as needed for comprehensive patient management plans.
  • Expedited prescription refills for patients under the supervision of healthcare providers, reducing medication lapses.
  • Enhanced patient care by efficiently managing medical records and coordinating appointments.
  • Reviewed physician's calendar and scheduled patient appointments by telephone and in-person.
  • Coordinated with appropriate administrative staff to address clinical, operational, and financial questions.
  • Called and faxed pharmacies to submit prescriptions and refills.
  • Utilized effective communication and active listening skills when interacting with physicians, nursing staff, and patients.
  • Performed medical records management, including filing, organizing and scanning documents.
  • Answered telephone calls to offer office information, answer questions, and direct calls to staff.

Education

Masters of Science - Biomedical Sciences

A.T. Still University - AZ School of Health Scienc
Mesa
07.2023 - Current

Some College (No Degree) - Post-Baccalaureate Studies

Oakland Community College
Bloomfield Hills, MI
08.2015 - 07.2021

Bachelor of Science - Brain, Behavior, And Cognitive Sciences

The University of Michigan
Ann Arbor
08.2008 - 12.2012

Skills

Coordinating site operations

Interdepartmental Collaboration

Data Collection

Quality Control

Software

Microsoft Applications

PC

Apple

Timeline

Masters of Science - Biomedical Sciences

A.T. Still University - AZ School of Health Scienc
07.2023 - Current

Clinical Research Associate

Henry Ford Health
09.2022 - Current

Clinical Assistant

Michigan Spine And Brain Surgeons
06.2022 - 10.2022

Some College (No Degree) - Post-Baccalaureate Studies

Oakland Community College
08.2015 - 07.2021

Bachelor of Science - Brain, Behavior, And Cognitive Sciences

The University of Michigan
08.2008 - 12.2012
Aisha TaborClinical Research Associate