Department of Clinical Research (DCR)

Job offers

We currently have the following vacancies:

03.05.2024 – Duties and responsibilities

Develop and implement a comprehensive project plan with other IMCI-PLUS consortium partners in Europe and Africa that includes all project phases, from initiation to closure, ensuring alignment with the study protocol and objectives and reporting requirements
Monitor project progress and performance, implementing necessary adjustments to meet project objectives and timelines
Manage project risks, including the development of contingency plans
Serve as the primary liaison between the project sponsor (DCR) and consortium partners, regulatory authorities, and other relevant stakeholders.
Ensure planning and implementation/delegation of all Sponsor-related tasks in adherence to ethical standards, and good clinical practice (GCP) guidelines throughout the study.
Oversee the research assistants and other trial staff involved in the project, with coordination of all staff at all locations of the study
Oversee the budget and financial activities representing DCR as the Sponsor
Prepare and present comprehensive and complex project reports

16.02.2024 – Zur Verstärkung unseres Teams suchen wir per 01.06.2024 oder nach Vereinbarung ein:e Study Nurse oder Studienassistent:in.