The Just in Time GCP Team
At Just in Time GCP (JiT), our team members are integral to our mission of delivering top-tier GCP compliance and clinical research consulting services. This month, we’re shining the spotlight on one of ours, Ralf Brooks, who joined the JiT Team just four months ago, in July of 2024. Ralf’s expertise in Good Clinical Practice (GCP) compliance, quality management systems, and clinical research continues to enhance our clients’ success.
Why did you decide to work at Just in Time GCP?
“I joined JiT because it offered the unique opportunity to be involved in a variety of services while collaborating with cross-functional teams. I was also excited about working with multiple clients across the clinical research industry, tailoring solutions to meet each organization’s unique needs. This diversity allows for significant personal growth in GCP compliance and the chance to expand my knowledge across various aspects of the field.”
How would you describe your job as a GCP Consultant at JiT?
“As a GCP consultant, I help clients navigate the challenges of GCP compliance and clinical research. My role involves listening to their struggles, assessing their current processes, and guiding them toward future states that comply with GCP regulations. I also help them develop sustainable quality management systems to maintain long-term compliance in clinical trials and operations.”
What do you want people to know about your job at Just in Time GCP?
“Our industry is evolving rapidly, especially as technology enhances quality management systems. The advancements we support in clinical research contribute to improved patient outcomes by enabling new therapeutics and medical devices to reach the market faster. Ensuring patient rights, safety, and welfare is at the core of what we do. I take pride in being part of a team focused on continuous improvement and quality assurance across the clinical research landscape.”
How has your experience helped you excel as a GCP Consultant at JiT?
“With a career spanning direct patient care, information technology, and over 18 years in clinical research, I’ve been exposed to quality initiatives from multiple perspectives—clinical, operational, safety, and compliance teams. This broad experience allows me to approach GCP compliance with an understanding of the various stakeholders involved, ultimately facilitating more effective quality management and regulatory adherence.”
At Just in Time GCP, we’re proud of Ralf’s contributions to GCP compliance consulting and his commitment to helping our clients succeed in the evolving world of clinical research. If you’re looking for expert guidance in clinical trial compliance, quality assurance, or regulatory consulting, Contact Just in Time GCP today to learn more about our services and click here to learn about our job openings.
