CTC-series: Meet our people. Part 8 – Björn Schultze (MD) is a resident physician in general medicine

Transitioning from clinical practice to clinical research can be both challenging and exciting. Meet one of our physicians at Clinical Trial Consultants (CTC), who shares his journey from primary care in Örebro to a dynamic new career path in clinical research.

After several years in primary care in Örebro, I developed a growing interest to explore new professional horizons. When relocating to Uppsala four years ago, the chance arose to join Clinical Trial Consultants (CTC). Despite not having been active in clinical studies before, I was aware of the company being a big player in life-science and a leading player in clinical research.

One of the most significant challenges I encountered early on was adapting to the dual responsibility of ensuring patient safety while adhering strictly to international clinical study regulations. My role shifted from treating patients to acting as an investigator, which required careful balancing. Fortunately, CTC provided extensive support and structured training that made the transition smooth.

“As a physician, I’m involved in the entire process—from protocol development and execution to final reporting.”

My current role at CTC significantly differs from my previous clinical work. While primary care was heavily appointment-based and relatively predictable, clinical research offers incredible variety. Tasks range from monitoring patients post-dosing and screening study participants to developing protocols and collaborating with external consultants. Administrative duties such as data reviews and handling unexpected issues add further diversity.

Among the many projects I’ve participated in, the collaboration with Dicot Pharma stands out as especially rewarding. Being involved from the earliest molecular stages through to Phase 2 trials across our entire Site Network, including our sister clinic in the Netherlands, has been inspiring. The close collaboration within the CTR group and the opportunity to work with passionate startup pharmaceutical companies contribute to a dynamic and enriching environment.

My clinical background has proven to be very useful in clinical research. My experience from primary care, handling diverse symptoms and patient profiles, contributes to my clinical assessment skills, which are just as important in a clinical research setting as they are in standard clinical work.

Ultimately, what I find most rewarding about working in clinical research is the breadth and variety of projects. Each study allows me to engage deeply—from protocol development to execution and final reporting—across various therapeutic areas ranging from Alzheimer’s disease to infant colic. This constant diversity ensures continuous learning and professional growth.