Katie Carty Email & Phone Number

Texas, United States

Dallas-Fort Worth Metroplex

Dallas, Texas

• Manage staff including interviewing, hiring, course of action on salary, professional development, and goal setting. • Manage staff performance and implement coaching and mentoring, corrective action, and terminations. • Manage site operations and provide supervision of all clinical and administrative aspects of a clinical trial to ensure delivery of targets and high quality.• Responsible for cost efficiencies within the site and collaborate with Team members on our vendor contracts.• Oversee site schedule and participant recruitment activities to ensure highest resource utilization.• Evaluate and implement operational strategies to enhance efficiency, provide competitive advantages, and improve overall profitability of the site.• Ensure site and site staff follow the company quality framework, guidelines, and international standards.• Collaborate with other departments including budgets and contracts, source, feasibility, regulatory, and study build and management to ensure customer satisfaction

Plano, Texas

Plano, Texas

Cincinnati, Ohio

• Maintained a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, tests, procedures, laboratory information, and drug accountability requirements.• Acted as a technical resource to less experienced research coordinators; answered questions, provided work samples or other assistance and support as needed.• Pre-qualified study participants. Met patient, reviewed medical history and informed consent process. Referred patients to other professionals as needed. Coordinated laboratory technician visits. Made final pre-study call to participants to relate acceptance and next steps.• Completed study documentation, including electronic case report forms.• Coordinated and conducted patient care visits and assured all procedures were conducted in compliance with the clinical protocol. Maintained patient safety assessed feedback from the patient and referred them to other professionals as needed. Dispensed study medications and completed drug accountability.• Interacted with the Investigators and Study Sponsors as needed to assure patient received appropriate medical evaluation and care.• Interacted with Clinical Research Associates to facilitate the sponsor monitoring and database clean-up process.• Attended sponsor Investigator/Study Coordinator meetings as needed for assigned protocols.• Conducted clinical research in compliance with all applicable regulations and complied with Good Clinical Practices.• Collected and processed laboratory samples, and obtained EKGs and vitals.

Cincinnati Area, Ky

Cincinnati Area, Ky

Cincinnati Area, Ky

Cincinnati Area, Ky