As a Site Activation Lead at ICON plc, I play a pivotal role in the successful initiation and execution of clinical trials across various phases, from I to IV, for both drug studies and medical devices. My primary responsibility is to serve as the main...
As a Site Activation Lead at ICON plc, I play a pivotal role in the successful initiation and execution of clinical trials across various phases, from I to IV, for both drug studies and medical devices. My primary responsibility is to serve as the main point of contact for sponsor relationships, ensuring that communication flows smoothly and that expectations are consistently met. This involves not only managing site activation timelines but also fostering strong partnerships with sponsors, which is reflected in our consistently high satisfaction scores.
In my current role, I am deeply involved in cross-functional collaboration, working closely with project teams to optimize the accelerated delivery of clinical projects. My expertise in risk management and mitigation allows me to identify potential challenges early on and implement effective solutions, ensuring that projects remain on track and within budget. My organizational skills are complemented by my ability to adapt to changing circumstances, which is crucial in the fast-paced environment of clinical research.
I thrive on challenges and am always seeking opportunities for innovation within the study start-up process. My quick learning ability enables me to stay ahead of industry trends and regulatory changes, which is essential for maintaining compliance and driving project success. As I explore new opportunities as a Study Start-Up Manager, I am eager to leverage my skills in budget negotiation, teamwork, and data analysis to contribute to impactful research that advances public health.
