Summary
Overview
Work History
Education
Skills
References
Timeline
Generic

Dr. Bradley Shinn

Mannford,OK

Summary

Regulatory science and clinical research professional with advanced training in health care administration, legal studies, and FDA policy. Skilled in documentation, compliance, and trial support, with a strong foundation in regulatory frameworks and stakeholder communication. Entrepreneurial, systems-minded, and quick to execute—bringing precision, adaptability, and a launch-ready mindset to fast-paced environments.

Overview

15
15
years of professional experience

Work History

Clinical Research & Regulatory Affairs Specialist (Aspiring)

Self-employeed
Mannford, OK
01.2021 - Current
  • As a dedicated professional with a strong academic foundation in clinical research and regulatory affairs, I am eager to apply my knowledge and analytical skills to ensure medical devices and pharmaceuticals meet global regulatory standards.
  • With a commitment to continual learning and professional development, I seek to contribute to the research and development process by integrating regulatory compliance from the outset.
  • My goal is to support product innovation while upholding the highest standards of safety and efficacy, leveraging my understanding of regulatory frameworks to facilitate successful market entries and benefit public health.

Team Member II

Follett Higher Education Group
Tulsa, OK
10.2015 - 11.2019
  • Resolved financial discrepancies and maintained accurate transaction records, contributing to audit readiness and operational transparency.
  • Designed and delivered onboarding and compliance training for new hires, reinforcing adherence to internal policies, and regulatory expectations.
  • Supported documentation workflows and procedural updates, laying the groundwork for scalable, policy-driven operations.

Course Materials Manager

Follett Higher Education Group
Tulsa, OK
11.2010 - 11.2014
  • Led a compliance initiative that aligned store operations with budgetary, sales, and inventory standards, resulting in 115% of projected enrollment sales.
  • Mentored and supervised a team of three, fostering a collaborative environment, and ensuring consistent delivery of high-quality services.
  • Managed scheduling and performance tracking, optimizing resource allocation, and supporting audit-ready documentation practices.

Education

Doctor of Health Care Administration -

Oklahoma State University
Stillwater, OK
05.2024

Master of Regulatory Science & Health Innovation -

Arizona State University
Tempe, AZ
05.2021

Master of Legal Studies - Oil, Gas, & Energy Law Concentration

University of Oklahoma
Norman, OK
05.2018

Skills

  • Skills
    Regulatory documentation & FDA submissions
    Clinical research coordination & trial support
    Global medical device & pharmaceutical regulations
    Human subject protection & adverse event reporting
    SOP development, policy review & audit readiness
    Compliance, risk mitigation & contracting familiarity
    Microsoft Office (Word, Excel, Outlook, PowerPoint)
    Project management & workflow optimization
    Data accuracy, reference tracking & trend analysis
    Time management & organizational efficiency
    Written communication, team collaboration & stakeholder engagement

References

References available upon request.

Timeline

Clinical Research & Regulatory Affairs Specialist (Aspiring)

Self-employeed
01.2021 - Current

Team Member II

Follett Higher Education Group
10.2015 - 11.2019

Course Materials Manager

Follett Higher Education Group
11.2010 - 11.2014

Doctor of Health Care Administration -

Oklahoma State University

Master of Regulatory Science & Health Innovation -

Arizona State University

Master of Legal Studies - Oil, Gas, & Energy Law Concentration

University of Oklahoma

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