Sena Oswalt,

Sena Ostwalt is a Clinical Research Coordinator with over seven years of experience in
clinical research, supporting preclinical and Phase I–III studies. She holds a Associate
in Nursing Degree and brings a strong clinical and operational background to the
coordination and oversight of clinical trials.

Her experience includes study start-up and close-out, participant recruitment and
screening, informed consent, safety monitoring, data collection, investigational product
management, and regulatory submissions. She has supported early-phase feasibility
and safety studies as well as later-phase efficacy and long-term follow-up studies
across multiple therapeutic areas. Her work has included complex protocols requiring
specialized procedures, strict eligibility criteria, and close investigator oversight.

Sena has supported sponsor and CRO monitoring visits, maintained regulatory and
electronic trial master files, and implemented electronic systems and standardized
workflows to ensure compliance with Good Clinical Practice and regulatory
requirements.

Sena has a focused interest in integrative and psychedelic research, with an emphasis
on participant safety, protocol adherence, and data integrity. She supports research
models that integrate rigorous clinical oversight, structured preparation, and post-
treatment follow-up to ensure ethical and compliant study conduct.

At the Institute for Integrative Therapies, Sena supports the development and execution
of clinical trials, contributing to the establishment of research infrastructure that
prioritizes safety, quality, and regulatory compliance.