* Worked with doctors and medical researchers throughout the US to assist with research
projects and clinical trials from phase 1 - 4.
* Worked with sponsors to create abstracts, study designs, protocols, and final reports for
publication.
* Assisted in data collection, sorting, and documentation of clinical information within the
constraints of the project.
* Managed resources, budgets, and timelines to ensure that all undertaken projects could be
managed effectively and efficiently.
* Work with CROs, third party vendors, and field CRAs to ensure compliance with study
protocol.
* Managed projects simultaneously with multiple teams ranging from 2 - 10 contractors to
ensure the customer's milestones and project deliveries were met.