Helen Thut Email & Phone Number

Basel, Switzerland

As GMP (Good Manufacturing Practice) Laboratory Coordinator I coordinate GMP manufacturing activities of the Innovation Focus Cell Therapies (IFCT), a multidisciplinary platform of the University Hospital Basel which provides and develops cell therapy programs to fight cancer and infectious diseases. My job includes coordinating between different GMP manufacturing teams, the GMP Facility for Advanced Therapies DBM and the clinic in order to enable the production of cell products administered to… Show more As GMP (Good Manufacturing Practice) Laboratory Coordinator I coordinate GMP manufacturing activities of the Innovation Focus Cell Therapies (IFCT), a multidisciplinary platform of the University Hospital Basel which provides and develops cell therapy programs to fight cancer and infectious diseases. My job includes coordinating between different GMP manufacturing teams, the GMP Facility for Advanced Therapies DBM and the clinic in order to enable the production of cell products administered to patients within the scopes of clinical phase I-II trials. In addition, I am Quality Control Manager for different cell therapy products of the IFCT by ensuring that the quality of the manufacturing processes and final cell therapy products meet all GMP standards. Show less

Basel, Basel-Town, Switzerland

My position as a clinical research coordinator included working with investigators and sponsors to provide patient care within the scopes of interventional clinical phase I-IV trials for cancer patients. I learned to maintain GCP (Good Clinical Practice) compliance with protocols covering patient care, clinical trial operations and regulatory guidelines. Collection of data by following research protocols, operations manuals and case report form requirements was done on a daily basis. Lastly, my… Show more My position as a clinical research coordinator included working with investigators and sponsors to provide patient care within the scopes of interventional clinical phase I-IV trials for cancer patients. I learned to maintain GCP (Good Clinical Practice) compliance with protocols covering patient care, clinical trial operations and regulatory guidelines. Collection of data by following research protocols, operations manuals and case report form requirements was done on a daily basis. Lastly, my work also entailed the optimization of processes in the clinical trial team and drafting SOPs. Show less

Master Of Science - Ms, Microbiology And Immunology

For my master’s thesis in Prof. Manfred Kopf’s Lab (Dept. of Molecular Health Sciences, ETH) I investigated the role of three main.

Bachelor Of Science - Bs, Biology

Education record