Monitoring of mainly Investigator Initiated Clinical Trials

Main responsibilities: Ensuring inspection readiness of eTMF; Supporting site managers and monitors; Reporting to clinical sites; Follow-up of queries from CRF Angio CoreLab

Main responsibilities: Lead the implementation of Veeva Vault eTMF; Act as Veeva Vault eTMF system administrator (system configuration; end-user training and support); Support CTMs in daily tasks related to clinical trials with external vendors (CRO) and internal stakeholders; Generate study team agendas, meeting minutes; Ensure inspection readiness of eTMF; Track study budget, prepare and update purchase orders, manage study invoices; Update tracking/reporting and planning tools (e.g. MS… Show more Main responsibilities: Lead the implementation of Veeva Vault eTMF; Act as Veeva Vault eTMF system administrator (system configuration; end-user training and support); Support CTMs in daily tasks related to clinical trials with external vendors (CRO) and internal stakeholders; Generate study team agendas, meeting minutes; Ensure inspection readiness of eTMF; Track study budget, prepare and update purchase orders, manage study invoices; Update tracking/reporting and planning tools (e.g. MS Project); Coordinate and/or contribute to the set up and maintenance of Clinical Studies in ClinicalTrials.gov; Coordinate the requests and follow-up of clinical trial insurances Show less

Main responsibilities: Support CTMs in daily tasks related to clinical trials with external vendors (CRO) and internal stakeholders; Generate study team agendas, meeting minutes; Ensure inspection readiness of eTMF; Track study budget, prepare and update purchase orders, manage study invoices; Update tracking/reporting and planning tools (e.g. MS Project); Coordinate and/or contribute to the set up and maintenance of Clinical Studies in ClinicalTrials.gov; Coordinate the requests and follow-up… Show more Main responsibilities: Support CTMs in daily tasks related to clinical trials with external vendors (CRO) and internal stakeholders; Generate study team agendas, meeting minutes; Ensure inspection readiness of eTMF; Track study budget, prepare and update purchase orders, manage study invoices; Update tracking/reporting and planning tools (e.g. MS Project); Coordinate and/or contribute to the set up and maintenance of Clinical Studies in ClinicalTrials.gov; Coordinate the requests and follow-up of clinical trial insurances Show less

Management of human clinical trial; designing new projects aligned with businesses

Co-promoting PhD-student; designing, organizing, controlling, and carrying out human clinical trial; teaching

Writing medical ethical applications; designing, organizing, and carrying out human clinical trials in the field of food intake regulation; recruiting human subjects; collecting and analyzing data; writing manuscripts; teaching