Bringing a medical device or new therapy to market involves navigating a complex product lifecycle, including the collection and reporting of clinical evidence.

At QbD Clinical, we guide our clients through every step of this journey. As a clinical solutions provider, we offer a unique combination of global CRO services and consultancy. Our expertise extends to medical writing, technical documentation, clinical evidence, and performance studies for IVDs, ensuring comprehensive support throughout the entire process.

Clinical investigations are designed to evaluate the safety and performance of medicinal products in humans, including identifying any adverse reactions.

With the right clinical solutions and guidance, we ensure that the resulting data is of the highest quality, fully compliant with regulatory standards, and delivered on time, helping to avoid costly delays and setbacks.

Career opportunities within Clinical solutions cover various aspects of clinical research. As a Clinical Trial Assistant (CTA), Clinical Research Associate (CRA), or Clinical Project Manager (CPM), you will support, manage sites, or lead projects across different phases and therapeutic areas of clinical trials.

If you're a Medical Writer, you’ll be responsible for regulatory and research documents, including literature reviews, clinical evaluation reports, and study protocols. For those more focused on Clinical Performance Studies for IVDs, we offer roles as Clinical Performance Studies Experts.

Do you have a Master’s or PhD in Biological, Pharmaceutical, or (Para-)Medical Sciences? Are you interested in clinical research, regulations, and quality? A career as a Clinical Consultant might be the perfect fit for you, where you’ll be part of the clinical evaluation process for innovative medicinal products.

Check our Young Potential Program