Clinical Trial Assistant@TRIUM

TRIUM Clinical Consulting, part of the QbD group, continues to grow and we are looking for a new colleague who will support us as a dedicated CTA. Main Purpose The Clinical Trial Assistant is responsible to assist the Clinical Research Professional (CRP) in the conduct of clinical studies and TRIUM management in the daily management […]

Medical Regulatory Writer

WHAT ARE YOUR MAIN RESPONSIBILITIES?  The Medical Writer is responsible for authoring, reviewing and editing clinical trial-related documents (including regulatory documents) and 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. […]

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? Do you want to be surrounded by fantastic colleagues in an authentic and growing company and be one of our ambassadors? You might be the Clinical Project Manager we are looking for at TRIUM Clinical Consulting, part of the QbD group!

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? Do you like to perform monitoring visits in hospitals? Do you want to be surrounded by fantastic colleagues in an authentic and growing company and be one of our ambassadors? You might be the Clinical Research Associate we are looking for at TRIUM Clinical Consulting, part of the QbD group!