Sofie Lemmens Email & Phone Number

Voeren, Flanders, Belgium

Maastricht En Omgeving, Nederland

Monitoring of mainly Investigator Initiated Clinical Trials

Maastricht En Omgeving, Nederland

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

Lausanne En Omgeving, Zwitserland

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

Région De Lausanne, Suisse

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

Région De Lausanne, Suisse

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

Région De Maastricht, Pays-Bas

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

Région De Maastricht, Pays-Bas

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

Initial Teacher Training Course, Chemistry And Biology

Master'S Degree, Biomedical Sciences, Clinical Molecular Sciences

Bachelor'S Degree, Biomedical Sciences

Education record