Summary
Overview
Work History
Education
Skills
Publications
Accomplishments
Timeline
Generic

Nathaniel Tyler

Portland

Summary

Accomplished Clinical Research Associate with nearly three years of experience performing and documenting pre-study site evaluations, regulatory document collection, interim monitoring and study close-out visits. Diligent in performing studies aligned with good clinical practices, study-specific requirements and clinical monitoring plans. In-depth knowledge of company procedures, regulatory requirements and quality standards. Adept at addressing ethical challenges, optimizing patient recruitment, and mentoring team members to achieve trial objectives.

Overview

6
6
years of professional experience
2018
2018
years of post-secondary education

Work History

Clinical research associate II (CRA II)

IQVIA
10.2023 - Current
  • Oversee complex site portfolios in CVRM, and liver disease, ensuring protocol compliance and high data quality.
  • Delivered comprehensive training to CRAs on advanced patient recruitment strategies, improving site enrollment rates.
  • Mentor junior CRAs and provide real-time guidance to enhance monitoring practices and professional development.
  • Conduct risk-based monitoring visits, resolving site issues efficiently to maintain adherence to study timelines.
  • Collaborate with site investigators to implement corrective actions and improve operational performance.
  • Consistently meet or exceed all performance metrics and KPIs, including site visit completion, query resolution timelines, and protocol compliance rates, ensuring high-quality clinical trial execution.

Clinical research associate I (CRA I)

IQVIA
03.2022 - 10.2023
  • Managed multiple sites for Alzheimer’s and diabetes studies, establishing robust relationships with investigators and site teams.
  • Supported regulatory submissions and compliance efforts, ensuring adherence to GCP, ICH, and sponsor requirements.
  • Performed data review and query resolution to maintain database accuracy and integrity.
  • Regularly achieved key performance metrics, including timely completion of monitoring visits and query resolutions, contributing to successful trial progression.

Lead & Clinical research coordinator (CRC)

OHSU
04.2019 - 12.2020
  • Company Overview: Dermatology
  • Directed onboarding and training for new research staff, fostering a high-performing team.
  • Coordinated complex trials, including pediatric and adult dermatology studies, integrating trial processes with standard care workflows.
  • Managed patient recruitment, biospecimen handling, and protocol-mandated procedures for over 10 industry-sponsored trials.
  • Conducted thorough documentation in EPIC, ensuring compliance and facilitating audit readiness.

Education

B.S. - Cellular And Molecular Biology

Western Washington University
Bellingham, WA
08-2017

Skills

  • Risk-based monitoring and site management
  • Therapeutic area experience: CVRM, liver disease, Alzheimer’s, diabetes, dermatology
  • Protocol compliance and regulatory adherence (GCP, ICH, FDA)
  • Patient recruitment and retention strategies
  • Advanced knowledge of KPIs and metrics tracking
  • Data query resolution and source data verification
  • Clinical documentation
  • Quality control
  • Clinical data management

Publications

Clark, K. M., Freeman, K. A., Richardson, K., Grzesek, K., Craven, S., Tyler, N., Al-Uzri, A., Internet use and health literacy among children with chronic kidney disease and their caregivers., 04/19, Poster session presented at the Pediatric Academic Societies Meeting, Baltimore, MD

Accomplishments

    IQVIA Innovation Award, 2024

Timeline

Clinical research associate II (CRA II)

IQVIA
10.2023 - Current

Clinical research associate I (CRA I)

IQVIA
03.2022 - 10.2023

Lead & Clinical research coordinator (CRC)

OHSU
04.2019 - 12.2020

B.S. - Cellular And Molecular Biology

Western Washington University

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