Emily Koller
Project Management | Clinical Trials | Avid Brazilian Jiu Jitsu Practitioner
- Role
- Clinical Trial Manager at Medpace
- Location
- Dallas-Fort Worth, TX, US
- LinkedIn followers
- 500 followers
About Emily Koller
I am a high-achieving professional with over a decade of experience in managing projects in research and industry environments, and two years of clinical project management experience. My career has allowed me to excel in both independent work and collaborative, cross-functional teams, successfully leading projects from inception to completion. Currently, I am focused on advancing my career in project management, where I aim to tackle problems, identify and mitigate risks, and enhance efficiency, all while maintaining awareness of the broader objectives. Throughout my career, I have cultivated a robust set of leadership, interpersonal, and communication skills, equipping me for success in a dynamic and fast-paced setting.Outside of my professional commitments and responsibilities, I am an avid supporter of career development and encouraging other professionals to be self-advocates. Some hobbies I pursue in my free time are Brazilian Jiu Jitsu, hiking, and reading. Let\'s connect!Skills, talents, and abilities: Project Management | Cross-Functional Team Leadership | Interpersonal Skills | Collaborative Problem Solving | Risk Management | Collaboration | Mentorship | Adaptability
Experience
Clinical Trial Manager
Oct 2024 — Present · Dallas-Fort Worth, TX, US
Oversee the daily operations for multiple global, Phase clinical trials in compliance with ICH/GCP guidelines, company SOPs, client requirements, and local regulations. •Act as the client’s point of contact for operational project-specific concerns and project deliverables. •Lead routine client meetings and site calls, utilizing presentation materials as needed.•Strategize to meet initiatives, oversee risk assessment, and implement mitigations. •Facilitate cross-functional oversight of program team members to ensure deliverables are provided within specification and timelines. •Ensure site quality by directly supervising project Clinical Research Associates and their deliverables.•Monitor completion of required project-specific training and disseminate lessons learned to the team. •Review and offer feedback on the study protocol and cross-functional documents and collaborate in the development of operational project plans.•Maintain a comprehensive understanding of the protocol, therapeutic area, and indication. •Participate in the management of and foster communication with study vendors.•Use proprietary Project Management system and numerous third party systems for study oversight.
Education
University of Florida
Bachelor's degree, Interdisciplinary Studies: Neurobiological Sciences
2011 — 2015
University of Florida
Doctor of Philosophy - PhD, Biomedical Sciences - Neuroscience
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