Successfully coordinating and managing up to 11 clinical research studies at a time throughout their full life cycle
from subject recruitment to study completion.
Project Management 26 Clinical Trials 9 Federal Research Grants Technology Savvy / EDC Proficient Regulatory Documentation IRB / FDA Submissions Neurocognitive CRF's Lab Operations Procedures Research
Subject Recruitment Develop Grant / Study Budgets
I get email after email after email from people that are interested in being subjects, so
subject recruitment is not going to be an issue.
Responsible for contract negotiations, regulatory compliance,
subject recruitment, enrollment through study closure.
Developed study design, budgets,
subject recruitment, testing protocols and contingency planning.
Tags for this Online Resume: clinical study coordination,
subject recruitment, inclusion and exclusion criteria for clinical study, drug accountability and reconciliation, source document review and update, assist with TMFs, Pre-Clinical research studies, blood collection, processing and shippment from sunjects