Jhenelle Hall

Responsible for creating and maintaining study documentation, preparing regulatory submissions, and implementing study protocols as directed by the principal investigator. Acts as the primary contact for study participants, managing inquiries and keeping them informed on study progress. Oversees inventory and supply management, collects and processes specimens, and inputs data into electronic systems. Collaborates effectively with research team members and contributes to reporting on study activities and outcomes.

Key responsibilities include performing medical diagnostic tests, collecting and processing blood and urine samples per protocol, interacting professionally with subjects and staff, maintaining laboratory inventory, sanitizing and stocking treatment and exam rooms, disposing of biohazard waste according to OSHA requirements, troubleshooting study issues, communicating relevant concerns to the Site Lead and Site Manager, maintaining source documentation, and ensuring timely data entry into the CTMS. Additional administrative tasks may be required.

Responsibilities include conducting medical tests, collecting and processing blood and urine samples, and coordinating recruitment, enrollment, and follow-up care. The role involves liaising between sponsors, regulatory agencies, patients, and investigators, performing data verification and quality control, maintaining research certifications (GCP and IATA), and managing IRB and regulatory paperwork.

Responsibilities include overseeing patient care, coordinating appointment scheduling, and conducting team huddle meetings. Assign patients to team members while ensuring assistance with activities of daily living (ADLs), transfers, and ambulation. Document care plans and maintain daily reports. Additionally, manage supply inventory, assist with medical procedures, and enforce safety protocols through proper PPE usage.