Summary
Overview
Work History
Education
Skills
Timeline
Generic

Ikram Hassan

Columbus,OH

Summary

Clinical Research Coordinator with progressive experience across multiple clinical departments through a centralized Float CRC role within a Clinical Trials Management Organization. Demonstrated expertise in cross‑departmental study support, quality oversight, and audit readiness, with hands‑on experience conducting full‑scope audits of FDA‑regulated studies. Adept at adapting rapidly to diverse protocols, teams, and patient populations.

Overview

8
8
years of professional experience

Work History

Float Clinical Research Coordinator

The Ohio State University – Clinical Trials Management Office
Columbus, OH
05.2025 - Current
  • Served as a Float CRC across multiple non‑cancer departments, supporting a wide range of therapeutic areas, protocols, and investigator teams.
  • Independently onboarded to new departments and trials, quickly adapting to varying workflows, protocol requirements, and sponsor expectations.
  • Screened patient records, recruited, consented, and enrolled participants in accordance with protocol, IRB, and regulatory requirements.
  • Coordinated and scheduled study visits, imaging, procedures, and diagnostic testing across multiple clinic environments.
  • Administered and scored standardized diagnostic, psychological, and behavioral assessments.
  • Supported multiple concurrent protocols (7–8 on average) across device, drug, and registry trials, ensuring protocol compliance and data quality across diverse study designs.
  • Collected, processed, and shipped biological specimens per protocol and IATA guidelines.
  • Collaborated with investigators, regulatory staff, and research leadership to ensure ongoing protocol compliance and data integrity.
  • Lead Quality Management Program (QMP) audits, conducting annual full‑scope audits of FDA‑regulated studies across multiple CCRM departments.
  • Identified regulatory and documentation gaps, draft audit findings, and supported corrective and preventive actions.

Clinical Research Coordinator

The Ohio State University – Department of Neurology
Columbus, OH
04.2023 - 05.2025
  • Recruited, consented, and enrolled participants in neuromuscular research studies.
  • Coordinated longitudinal study visits and patient education for participants and caregivers.
  • Participated in site qualification, initiation, and close‑out visits.
  • Documented and reported adverse events and serious adverse events to sponsors and regulatory bodies.
  • Administered neurology‑specific assessments, including manual muscle testing and spirometry.
  • Collected, processed, and shipped biospecimens following protocol‑specific and IATA procedures.

Research Assistant

The Ohio State University – Department of Molecular Genetics
Columbus, OH
04.2019 - 01.2020
  • Assisted with data collection, extraction, coding, and analysis.
  • Supported day‑to‑day lab operations, equipment maintenance, and inventory management.
  • Created source documents to support consistent protocol execution and accurate data capture.

Research Assistant

Ohio University – Department of Psychology
Athens, OH
01.2018 - 01.2019
  • Supported behavioral psychology studies involving diverse participant populations.
  • Recruited, consented, and enrolled pediatric participants.
  • Completed CRFs and source documentation in compliance with human subjects research guidelines.
  • Built rapport with vulnerable populations to support ethical research participation.

Education

Bachelor of Science - Biology

The Ohio State University
Columbus, OH
12-2022

Skills

  • Electronic Data Capture (EDC) systems: Medidata Rave, Zelta, PharmaAccess, REDCap
  • Source document verification (SDV) and CRF review
  • Audit and monitoring support, including quality reviews and inspection readiness
  • Protocol compliance and ICH‑GCP adherence
  • Adverse event (AE) and seriousness assessment documentation support
  • Risk‑based monitoring (RBM) principles and data quality oversight
  • Biological specimen handling, processing, and shipment (IATA‑compliant)
  • Administration and documentation of standardized assessments (C‑SSRS, SVC)

Timeline

Float Clinical Research Coordinator

The Ohio State University – Clinical Trials Management Office
05.2025 - Current

Clinical Research Coordinator

The Ohio State University – Department of Neurology
04.2023 - 05.2025

Research Assistant

The Ohio State University – Department of Molecular Genetics
04.2019 - 01.2020

Research Assistant

Ohio University – Department of Psychology
01.2018 - 01.2019

Bachelor of Science - Biology

The Ohio State University