My professional tenure has been marked by a steadfast commitment to operational excellence, adaptable problem solving, and effective stakeholder management, including pharmaceutical companies, CROs, IRBs, and principal investigators. As a Clinical Research Coordinator, I honed my skills in clinical research site operations and overseeing multiple complex clinical trials requiring DSMB interactions and consistently met all protocol requirements and regulatory standards. As a Project Manager, I have further developed my ability to be a strategic thinker and collaborative communicator. These qualities are at the core of my leadership style and have proven essential in the highly effective and cohesive project teams and cross-functional efforts I have built and maintained.I am quite knowledgeable in conducting clinical trials from site qualification to closeout while adhering to internal SOPs, GCPs, ICH guidelines, and FDA regulations. I have successfully overseen and assisted on multiple clinical trials in various phases and met stakeholder expectations on all clinical trials.I also believe in continuous improvement and frequently seek out education opportunities, such as LinkedIn certifications and my current pursuit of PMP certification. I am fully committed to the innovative advancement of healthcare through clinical research and support of currently marketed medical therapies and devices.