Protocol-aligned visit support
Helping participants and teams move through study visits with clear next steps.
About us
Our team
Kyah Harding
Kyah Harding is Clinical Research Coordinator at Mood Institute, supporting study visits, documentation, and research-assistant workflows for PCORI programs NCT06713616 and NCT06725277. She has TMS technician experience on Magstim Horizon 2 and 3 under clinician-prescribed protocols, with GCP, HIPAA, REDCap, CPR, and Magstim training. English fluent; Mandarin proficient.
- Clinical Research Coordinator
- Research operations
- TMS experience
Kyah Harding is Clinical Research Coordinator at Mood Institute. She supports day-to-day research operations as a coordinator and research assistant, including participant communication, visit coordination, and documentation for public studies listed on ClinicalTrials.gov (NCT06713616 and NCT06725277).
She has TMS technician experience on Magstim Horizon 2 and 3 under clinician-prescribed protocols, with GCP, HIPAA, REDCap, CPR, and Magstim training. She is fluent in English and proficient in Mandarin.
Participants can ask Kyah about visit logistics and study procedures; the study team handles screening and eligibility review.
Qualifications
- Clinical Research Coordinator, Mood Institute
- Research Assistant support on public clinical studies
- TMS technician experience on Magstim Horizon 2 and 3 under clinician-prescribed protocols
- GCP, HIPAA, REDCap, CPR, and Magstim training
- Support for PCORI studies NCT06713616 and NCT06725277
- English fluent; Mandarin proficient
Clinical & professional focus
- Clinical research coordination and research-assistant visit support
- Study-visit communication, source documentation, and REDCap workflows
- Delegated assessments as trained and permitted under investigator oversight
- TMS technician support on Magstim Horizon 2 and 3 under clinician-prescribed protocols
Education & training
- B.S. Economics, Pre-Medical Track, Stony Brook University (expected May 2029)
How this role supports care
Careful documentation
Supporting accurate source records, REDCap workflows, and research operations standards.
Clear communication
Working in English and Mandarin so visitors can ask questions and understand next steps.
Research operations
- Clinical Research Coordinator
- Research Assistant
- TMS technician experience under clinician-prescribed protocols
Kyah Harding supports Mood Institute research operations as Clinical Research Coordinator and Research Assistant for public studies described on ClinicalTrials.gov, including PCORI programs NCT06713616 and NCT06725277.
Research activities are performed under investigator oversight and site procedures, with a focus on visit coordination, accurate documentation, participant-centered communication, and TMS technician support on Magstim Horizon 2 and 3 under clinician-prescribed protocols.
Research areas & focus
- Study-visit coordination and participant communication
- Source documentation and REDCap workflows
- Delegated assessments as trained and permitted
- TMS technician support on Magstim Horizon 2 and 3 under clinician-prescribed protocols
- PCORI NCT06713616 and NCT06725277 support
Research certifications & qualifications
- Good Clinical Practice training
- HIPAA compliance training
- REDCap training
- CPR training
- Magstim Horizon 2 and 3 TMS technician training
Affiliations
- Mood Institute — Clinical Research Coordinator
Related public studies
- NCT06713616PCORI Study: IV Ketamine vs Esketamine for Treatment-Resistant Depression
- NCT06725277OBSERVE Study: Real-World Outcomes in Depression Care
Study status and eligibility details are maintained on ClinicalTrials.gov. Contact the research team with questions about a listed study.
Published resources
Articles by Kyah Harding
Explore every Mood Institute resource attributed to Kyah.
What a TMS session is like at Mood Institute
A step-by-step look at check-in, room setup, the treatment chair, and check-out.
Patients & FamiliesHow a Mood Institute visit typically flows
What happens from the moment you arrive until the team confirms what comes next.
Patients & FamiliesTMS visit cadence for referring clinicians
How to set expectations about visit rhythm, technician support, and care-team updates.
Referring ProvidersWhat referring clinicians can tell patients about TMS visits
Clear talking points for setting expectations before a TMS or research-related visit.
Referring ProvidersHow a clinical research coordinator supports study visits
What a coordinator may help with before, during, and after a research visit.
Research ParticipantsDelegated assessments in Mood Institute research visits
What a delegated assessment may feel like and which questions to ask beforehand.
Research ParticipantsTMS technician workflows in research operations
Verification questions for staffing, device experience, delegation, and visit documentation.
Research SponsorsDocumentation quality from CRC and research-assistant workflows
Questions sponsors can ask about source records, REDCap reconciliation, and review readiness.
Research Sponsors