About Me.
I am Shane Small, a Clinical Research Associate with over 12 years of experience in the clinical stage drug development industry. Throughout my career, clinical research has emerged as a dynamic field, providing me with opportunities to assume various roles across multiple therapeutic areas. I've had the privilege of collaborating with a wide array of colleagues and companies, enriching my expertise and reinforcing my belief in adaptability, effective communication, and lifelong learning.
My commitment to empathy, transparency, and exceptional support for stakeholders has set me apart when working as part of a team. I tackle challenges with adaptability and a readiness to meet study endpoints within timelines. In the fast-paced and evolving drug development industry, my ability to swiftly adjust to new challenges, regulations, and technologies is paramount. I am devoted to supporting clinical sites with a hands-on, transparent approach, ensuring every project meets its objectives. This dedication has been pivotal in my career, allowing me to make significant contributions to the advancement of medical science and patient care.
At the core of my professional ethos is effective communication. I pride myself on building strong, productive relationships with all stakeholders involved in the clinical trial process, from site coordinators and investigators to regulatory bodies and sponsors. My skill in clear, concise, and timely communication has been instrumental in navigating the complexities of drug development, ensuring project milestones are met with precision and efficiency.
My approach to clinical research is deeply rooted in continuous improvement and education. I believe there is always room to grow, learn, and enhance our skills and knowledge base. This belief has propelled me to seek out new learning opportunities consistently, keeping me at the forefront of the latest industry trends and methodologies. My unwavering dedication to advancing medical science through meticulous research underscores each project's unique challenges and objectives.
In summary, my career is a testament to a commitment to advancing healthcare, highlighted by a lifelong dedication to learning, effective communication, and adaptability. As I continue to explore new opportunities within clinical research, I am eager to leverage my skills and experiences to further the development of life-saving treatments.
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Proficiencies Include:
• Clinical Monitoring
• CRA Management and Resourcing
• Site Management and Guidance
• Quality Assurance
• Clinical Study Start-up
• TMF Management