Clinical Trial Assistant

QbD Clinical, part of the QbD group, continues to grow and we are looking for a new colleague who will support us as CTA. What do we expect from you as a Clinical Trial Assistant? The Clinical Trial Assistant is responsible to assist the Clinical Research Professional (CRP) in the conduct of clinical studies and […]

Medical Writer

The Medical Writer is responsible for authoring, reviewing and editing clinical trial-related documents scientific publications. He/she is responsible for presenting clinical data objectively in a clear, concise format and ensures timely delivery of these documents in accordance with all applicable quality and/or regulatory standards or requirements.   What do we expect from you as a […]

Clinical Project Manager

Do you want to make an impact as a Clinical Research Professional? Do you get energy from coordinating dynamic clinical trials with a quality-driven and pragmatic approach? Do you like to partner with many stakeholders? Do GCP ICH E6 R2 and ISO 14155 have no secrets anymore for you? You might be the Clinical Project […]

Clinical Research Associate

Do you want to make an impact as Clinical Research Professional? Do you want to protect the safety & well-being of subjects and guarantee data quality? Do you get energy from daily communication with investigators, study coordinators and study teams? Do GCP ICH E6 R2 and ISO 14155 have no secrets anymore for you? You […]

Come visit our booth at CPHI Barcelona 2023

Come to see the QbD Group at stand #3G73 at CPHI Conference in Barcelona. And after the conference…Eat & Connect with lifescience professionals at our QbD’s CPHI Networking Drink.