About Me

Dr. Janet Tingling

DBA, MBA, MS, BS, AS, AA

Dr. Janet Tingling - Director of Research, with expertise in managing all aspects of Clinical Trial Research, which includes SOP, GCP, quality improvement matrix, regulatory/ethical policies to ensure the integrity of the study, and grant writing.

She is also a collaborative and forward-thinker with over 11 years of progressive experience in Clinical Trials Research.

💼 My Professional Expertise

Over the years, I have led and supported various clinical trials, regulatory audits, and compliance programs across academic institutions, hospitals, and global research organizations. My expertise lies in developing audit-ready research programs, improving clinical documentation practices, and ensuring all study operations align with ICH-GCP, FDA, and IRB guidelines.

Some of my key strengths include:

Clinical Research Leadership: I manage complex, multisite trials while fostering collaboration between investigators, coordinators, and sponsors.
SOP Implementation & Training: I design SOPs tailored to regulatory expectations, and train teams to execute them with confidence and clarity.
Regulatory & Risk Management: I proactively assess risk factors and build compliance programs that meet HIPAA, FDA, EMA, and ICH standards.
Quality Improvement: I use data-driven KPIs to measure performance, identify process gaps, and optimize operational efficiency.
Mentorship & Leadership Development: I guide emerging professionals and cultivate leadership skills to build strong, resilient research teams.

These roles have not only refined my technical skills but also deepened my purpose: to create systems that are both regulatory-compliant and people-centered.

🔍 My Mission

I believe clinical research is about more than data points and documentation — it's about advancing human health through ethical, reliable, and well-executed trials. My mission is to be a catalyst for research excellence, helping organizations build stronger research frameworks, navigate evolving regulations, and elevate standards of care.

“Every successful trial begins with a foundation of ethics, education, and collaboration.”

🧠 Thought Leadership

In addition to my professional roles, I regularly publish articles and blog posts on topics like:

Best practices in clinical trial compliance
Using quality improvement frameworks in research
Preparing for regulatory audits
Developing SOPs that work in real-world settings
Mentoring research professionals for long-term impact

These insights are born from real experience — challenges I’ve faced, solutions I’ve designed, and lessons I continue to learn.