Associate Vice President of Accounting & Finance at ENCORE Research Group
Shannon Trull negotiate contract language and budgets with pharmaceutical companies and contract research organizations for seven clinical research sites. Review language in contracts with specific emphasis on indemnification, subject injury and informed consent. Review payment terms and pass-through expenses for each budget. Review contract amendments and prepared them for signature. Communicate procedure requirements and negotiate fees for specific testing with local hospitals and other third party vendors.…
Amanda Elwood, CCRP
Regulatory Specialist at Jacksonville Center for Clinical Research
Amanda Elwood is the Regulatory Manager at ENCORE Research Group. She is a Certified Clinical Research Professional responsible for handling regulatory compliance and study start-up for all eight ENCORE clinical sites.
Associate Vice President of Business Development
Jolenne Wolfer provides Business Development for eight Encore Clinical Research sites in the state of Florida. Site capabilities include multi-specialty Phase I through IV drug, device, investigator-initiated, and vaccine, both inpatient and outpatient trials. Current areas of expertise include cardiovascular, gastrointestinal, diabetes, weight loss, vaccines, CV surgery, infectious disease, women’s health, and PK/PD/FIH studies.