The CPMO coordinates the planning of translational research project in lines with LIH strategy and closely interacts internally as well as externally with clinical sites and other collaborators such as LNS, Uni.lu, etc.
CPMO centrally oversees the planning and implementation of all Clinical Research projects and programs.
Practically, CPMO takes charge of every step of clinical research projects (lead, design, setup, initiation, operation and closure) involving internal and external parties, ensuring deliverables are achieved and budgets met, and providing specific expertise and know-how in clinical research and biobanking.
Main point of contact for the various partners involved in Clinical Research projects, including clinicians and researchers
Link between the units of the TMOH to support translational programmes
Support private sponsors, researchers and investigators from other research institutions or hospitals in the setup (contract, admin, approvals, timelines, budget, etc.) and conduct of clinical research projects
Coordinate and manage a portfolio of life science/clinical research projects according to the contract/scope of work, protocol, budget (setup financial contracts and manage financial aspects during the projects) and fixed timelines
Supervise and assist regulatory submissions (national and international, to health authorities and research ethics committees) according to the applicable laws, administrative and regulatory requirements and obtain approvals
Support the participation in European consortia and grant applications