April Gregory-Snyder Email and Phone Number

Coordinate phase III double blind and open label extension cardiac amyloid drug trials.Screen, consent, and enroll patients into the studies.Obtain medical records and abstract health information.Schedule patients for tests and clinic appointments.Assess patients in clinic and maintain close follow-up via phone calls, email, and text.Coordinate with multiple disciplines for home care, periodic tests, scans, and lab draws.Maintain electronic data capture (EDC) records, perform data entry, record adverse events, and answer queries.Maintain regulatory and patient study documents.Proficient with RedCap, OnCore, Cerner, Medidata, and other study-specific platforms.Attend staff meetings, CRA monitoring visits, and sponsor educational meetings.

Founded and established not-for-profit recreational dance studio consisting of a six-person director collective.Knowledge of studio operations, finances, hiring of teaching staff, facility maintenance, public relations, student enrollment, newsletters, and annual schedule of classes and performance events.

Generate passive income through online sales of original written patterns.Manage small business details and customer service inquiries.

Screened, consented, and enrolled patients in various in-vitro diagnostic studies.Experience running multiple, often concurrent, short-term studies ranging from three months to two years.Performed collection and processing of subject specimens and shipped biohazardous samples.Extracted subject data from electronic medical records (EMR), maintained accurate source documentation, and entered data into EDC system.Operated core laboratory machines, point-of-care devices, and various instrumentation.Maintained regulatory and subject study documents.Attended site initiation visits, regular staff meetings, and monitoring visits. Experienced in Epic and Cerner EMR.

Various appointments 1998 to 2001, 2008 to 2011, 2016 to 2017Cultured, harvested, and analyzed human metaphase chromosomes for diagnostic cancer, constitutional blood, amniotic fluid, and tissue results.

Lead small team of research assistants in data collection and recording of trial data for Indiana site Phase III Covid-19 Vaccine Trial.Obtained and verified large volume of clinical trial data from electronic source documents.Maintained accurate and timely entry of trial data into Electronic Data Capture (EDC) system.Answered queries and met deadlines for focused reports from site CRA and central monitoring.Communicated and coordinated with site management and trial monitors.

Managed total care for two critical patients per shift, including assessments, vitals, blood gases, glucose levels, medications, IV fluids, therapeutic communication, and proper positioning.Maintained venous, arterial, and central lines, and monitored ventilators, and heart rhythms.Managed surgical drains, dressings, tracheostomy care, and skin care.Documented in electronic medical record and upheld confidentiality.

Obtained vital signs, measured intake and output, and obtained blood glucose checks.Performed periodic blood draws for labs.Performed patient ambulation and hygiene.Managed surgical dressings and drains.