Pamela Lackner

Clinical Research Coordinator III is experienced clinical research professional responsible for leadership planning, implementing, monitoring, and evaluating multiple clinical research protocols. This role manages multiple studies' daily operations, performs study coordination duties from protocol development and initiation to study close-out according to regulatory/sponsor guidelines, assures each study's integrity, and mentors less experienced Clinical Research Coordinators. The incumbent monitors and maximizes adherence to research standards and regulatory policies and approved operational procedures works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, manages study-related administrative and human resources tasks, facilitates across-the-board flow of information, and orchestrates study activities and personnel. Experienced, energetic, and solution-focused professional with a diverse background in Research administration for large patient-care projects. Ability to organize and adapt. Strong people skills and positive attitude. Demonstrate completion of milestones and deadlines. Multitasking, organizing, and recording data accurately produce quality work in healthcare management that meets ambitious standards and is looking to improve the quality of my deliverables and adhere to the highest moral principles and professional standards.