Manages the Clinical Research Program, Operations, financials, and Research Staff across the five locations. Collaborates with Sponsors, Clinical Research Organizations (CROs), and the US Oncology Network to facilitate clinical trial opportunities while overseeing all contract and budget negotiations.
Natasha Holt, CCRP
Collaborates in the development of research accountability standards, metrics, and quality for the Research Staff. Provides administrative support to the Clinical Research Manager and leadership team.
Andi Pollard, CCRC
Responsible for enrolling patients onto Phase I clinical trials, administering all medications to patients on Phase I trials, and providing/coordinating patient care while protecting the integrity of the clinical trial.
Responsible for enrolling patients on Phase II-IV clinical trials and providing/coordinating patient care while protecting the integrity of the clinical trial.
Jessica Nichols, CCRC
Emily Counts, CCRC
Dana Selvia, CCRP
Karen Everhardt, RN
Responsible for extrapolating data from source records for all clinical trials and submission to Sponsors and/or Clinical Research Organizations (CROs)
Responsible for managing all drug and lab kits for the Phase I-IV clinical trials
Leigh Anne Phan
Responsible for managing the regulatory for Phase I-IV clinical trials working closely with Institutional Review Boards (IRBs)