Open to opportunities

Rosy Engle

@rosyengle

Compliance and clinical research professional focused on ethical regulatory adherence, licensing oversight, and data-accurate trial operations.

United States

Message

What I'm looking for

I’m looking for a role where I can strengthen ethical, law-driven compliance and keep documentation audit-ready. I want to partner with teams, stay ahead of regulatory changes, and contribute to accurate, high-integrity clinical or operational outcomes.

I’m driven by a simple goal: help organizations operate ethically and within the law. As a Compliance Specialist, I manage multi-state insurance licensing compliance, prepare and track regulatory submissions, and maintain audit-ready documentation that protects both the company and its stakeholders.

Previously, I coordinated clinical research studies with a strong emphasis on protocol, timelines, and regulatory requirements. I recruited and screened participants, supported IRB submissions, ensured Good Clinical Practice (GCP) adherence, and handled investigational product accountability while keeping records accurate through electronic data capture and case report forms (CRFs).

My foundation includes long-term healthcare operations work as a Medical Scribe/Research Assistant, strengthening my attention to detail in source documentation, EMR input, and medical billing (ICD-10). Whether it’s compliance records or clinical documentation, I bring a consistent commitment to integrity, accuracy, and dependable follow-through.

Experience

Work history, roles, and key accomplishments

Current

Compliance Specialist

Current

Sycamore Specialty Underwriters LLC

Aug 2024 - Present (1 year 10 months)

Manage insurance producer, agency, adjuster, and surplus lines licensing across multiple states in accordance with DOI regulations. Prepare and track license applications, renewals, appointments, terminations, surplus lines filings, and maintain compliance records for audits and regulatory inquiries.

State DOI Filings Insurance Licensing Surplus Lines Audit Readiness Stamping Office Submissions

Senior Clinical Research Coordinator

Oakland Hills Dermatology

Aug 2023 - Aug 2024 (1 year)

Coordinated clinical research studies to ensure adherence to protocols, regulatory requirements, and timelines. Recruited and screened participants, scheduled study visits, supported IRB submissions, maintained GCP-aligned records, and managed investigational product accountability.

Good Clinical Practice (GCP)Clinical Trial Coordination Participant Recruitment & Screening IRB Submission Investigational Product Accountability SOP Development

Clinical Research Coordinator

ONYX Clinical Research

Feb 2023 - Jun 2023 (4 months)

Coordinated day-to-day research study activities, including protocol execution, subject recruitment, and informed consent. Maintained study databases in Excel, managed follow-up visits and assessments, documented communications and monitoring findings, and tracked investigational medicinal product documentation and temperature logger readings.

Excel Research Databases Subject Follow Up Scheduling Temperature Logger Monitoring

Medical Scribe/Research Assistant

Michigan Institute for Neurological Disorders (M.I.N.D)

Jul 2015 - Sep 2020 (5 years 2 months)

Documented patient histories and examinations, supported vitals and EMR updates, and tracked test results from external providers. Assisted during procedure clinics (Botox/Dysport/Xeomin/Myobloc), managed toxin trial data and patient education, supported billing using ICD-10, and supervised medical students and residents during clinic hours.

EMR Medical Documentation Botox Dysport Xeomin Administration Support Toxin Trial Data Management ICD 10 Coding