Stacey Boetto

Clinical Research Investigator

Dr. Stacey Boetto is a Principal Investigator with over 30 years of combined experience as a nurse and nurse practitioner. Dr. Stacey has worked in clinical research for five years, including three years in a Principal Investigator role. Her career has included diverse roles across different health areas, leading to a broad clinical background which informs her patient-centered approach to research.

Her interest in clinical research developed from a desire to contribute to evidence-based innovation. Since entering the field, she has supported a wide range of trials in areas such as Cardiology, Nutrition, Medical Devices, Sleep, Mood, Endocrine, and Women's Health. She is known for her commitment to research integrity, participant wellbeing, and high-quality data.

Alongside her role as Principal Investigator, she brings expertise in clinical trial management, regulatory compliance, nursing informatics, and medical writing. Her contributions extend to peer reviews, medical reporting, NFPA 1582 assessments, and community education. She has also supported practice start-ups and telehealth models and remains an active mentor to nurses and nurse practitioners through precepting and staff training initiatives.

Total Years of Experience: Over 30 years as a Nurse Practitioner and Nurse, with 5 years in clinical research, including 3 years as a Principal Investigator.

Career Journey: Dr. Stacey Boetto began her career as a nurse in Cardiac and ICU placements, where she developed a strong foundation in critical care and high-acuity patient management. Over the years, she expanded her clinical expertise across a wide range of specialties, including Pain Management, Post-Anesthesia Care (PACU). Her work also extended into Occupational Health, Ortho/Spine, Urgent Care, Hormone Replacement Therapy, and Weight Management. These experiences gave her a well-rounded perspective on patient care across different settings and life stages. This practical foundation eventually led her to clinical research, where she brings the same attention to detail, safety, and care that defined her early clinical work.

Clinical Trial Experience: Stacey has contributed to a wide range of clinical trials across multiple therapeutic areas, supporting studies from initiation through to completion. Her research experience includes trials in cardiology, oncology, nutrition, weight management, gastrointestinal health, and women’s health, as well as investigations involving medical devices, dental health, endocrinology, sleep, mood, and nutraceuticals. She has also worked on studies involving durable medical equipment (DME), bringing a practical understanding of both intervention-based and observational research settings.

Key Contributions: Providing clinical oversight, supporting data accuracy, leading participant visits, and maintaining regulatory standards. She also supports training initiatives and contributes to team development.

Collaborations: Dr. Stacey has worked with interdisciplinary teams of physicians, researchers, statisticians, and regulatory specialists to design and deliver compliant clinical trials. She has partnered with universities, healthcare organisations, and professional associations on research projects, education, and evidence-based practice initiatives. Her collaborations also include community health groups, government bodies, and pharmaceutical and biotech companies to advance policy, research, and patient care.

As Principal Investigator, Stacey is responsible for the clinical oversight of research studies, ensuring that all protocols are followed with precision and that participant safety and wellbeing are prioritised at every stage. Her role involves close collaboration with the research team to maintain high standards of care, data integrity, and regulatory compliance throughout each study.

Key Responsibilities:

Ensuring strict protocol adherence across all trial procedures and assessments
Monitoring participant safety and managing adverse events throughout the study
Maintaining data integrity through accurate, complete, and reliable data collection
Upholding regulatory compliance with all applicable guidelines and ethical standards
Coordinating day-to-day trial operations, including scheduling, resources, and stakeholder communication

Stacey Boetto

Clinical Research Investigator

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