Summary
Overview
Work History
Education
Skills
Timeline
Generic

OLANIKE ASUPOTO

Melrose,MA

Summary

Results-oriented Clinical Research Coordinator with three years of experience in managing and coordinating clinical trials across diverse therapeutic areas. Proficient in conducting participant recruitment, regulatory compliance, and data management while ensuring adherence to protocol and ethical standards. Adept at fostering community engagement initiatives to enhance participant retention and study awareness. Proven ability to collaborate with interdisciplinary teams and stakeholders to drive successful research outcomes. Strong communication and organizational skills coupled with a passion for improving healthcare delivery through rigorous clinical research.

Overview

3
3
years of professional experience

Work History

Clinical Research Coordinator II

Boston Medical Center
10.2022 - Current
  • Provide study support to manage under sourced trials
  • Responsible for the primary recruitment, data management, source documentation and adverse event monitoring
  • Support inclusive and diverse outreach by attending community events and implementing education initiatives within the Boston community.

Clinical Research Coordinator I

Dana-Farber Cancer Institute
01.2021 - 09.2022
  • Supports the research team in clinical trials using Good Clinical Practice
  • Responsible for the primary data collection and management of patient clinical information
  • Ensures timely collection of protocol related samples including shipment
  • Maintain regulatory binders
  • Ensures study compliance with all state, federal, and IRB requirements

Education

Masters in Public Health, Population Health Promotion -

Tufts University School of Medicine
Boston, MA
08.2024

Bachelor of Science in Biology -

University of Massachusetts
Boston, MA
08.2020

Skills

  • Strong knowledge of clinical research protocols and regulations
  • Proficient in data collection, analysis, and reporting Experience with electronic data capture systems and clinical trial management software
  • Excellent organizational and time management skills Ability to communicate effectively with healthcare professionals, study participants, and research team members
  • Understanding of Good Clinical Practice (GCP) guidelines and ethical considerations in research Ability to work independently and as part of a multidisciplinary team
  • Familiarity with regulatory requirements and IRB processes
  • Proficiency in Microsoft Office applications

Timeline

Clinical Research Coordinator II

Boston Medical Center
10.2022 - Current

Clinical Research Coordinator I

Dana-Farber Cancer Institute
01.2021 - 09.2022

Masters in Public Health, Population Health Promotion -

Tufts University School of Medicine

Bachelor of Science in Biology -

University of Massachusetts
OLANIKE ASUPOTO