Barbara Hubeli (Szczerba) Email & Phone Number

Zurich, Switzerland

Boudry, Neuchâtel, Switzerland

Main responsibilities:• Collaboration with Global Trial Mangers and other global study team members on Sponsor-Initiated Trials: Phase III CAR T - cell therapy and Phase Ib/IIa (Full Development) • Providing operational input on development, management, and maintenance of study deliverables• Creation and maintenance assistance of project documentation• Maintenance and input of clinical tracking information into CTMS• TMF and CRO’s TMF Oversight• Monitoring Visit Reports (SIV, IMV, COV) Review and ICF Review• Invoices approval• Safety Reports analyses• Routine anticipation, identification and resolution of potential issues and implementation of CAPAs• Utilized systems include: CTMS, TMF, EDC, IVRS, SIP

Zurich, Switzerland

Main responsibilities:• Design, set-up and management of an early phase clinical trial (study cohort: oncological patients resistant to immunotherapy, IIT) including development of full study documentation (e.g. Study Protocol, Protocol Amendments and ICFs) and eCRF design (SecuTrial EDC)• Design, set-up and management of non-interventional research studies (IITs) • Clinical Data Review• Clinical Biospecimen planning• Coordination of numerous research projects across clinical, academic and industry partners and main contact person for external partners (e.g., KOLs)• Responsible for communication (incl. document submission) with a local Ethics Committee • Developed site training materials and providing training to study personnel Main Achievements:• Builded up a clinical trial from the design phase till FPFV (March 2022)• Designed and funded (app. 0.5 Mo CHF from research grants) own research project and mentored PhD and MD/PhD students

Basel, Canton Of Basel-Stadt, Switzerland

Main responsibilities:• Support in developing processes and documentation necessary for the planning of clinical studies in compliance with applicable regulatory guidelines• Management of collaboration with external research partners• Providing scientific components for study protocol developments and clinical quality documentation• Preparation of internal scientific presentations, research manuscripts and review articles• Developing protocols and execute measurements of biological tissue specimens for nanomechanical measurements• Execution of measurements on reference hydrogels and research specimens using atomic force microscopyAdditional responsibilities as a Usability Engineer:• Conducting Cognitive Walkthrough method on different projects using SCRUM method• Assisting in preparing various stakeholders interview questionnaire and in conducting contextual interviews• Assistance in user interface design and executing design reviews

Basel, Switzerland

Charlottesville, Virginia, United States

Doctor Of Philosophy (Phd), Cancer Metastasis, Summa Cum Laude

Project: Dissection of circulating tumor cell cluster heterogeneity using single-cell DNA and RNA profiling. Research performed.

Master Of Science (Msc), Immunology

Fulbright Scholar Program Project: Type I interferons in the pathogenesis of Sjögren's Syndrome. A novel pre-clinical model was developed.

Bachelor Of Science (Bsc), Molecular Biology