KLIFO
Jessica Hansen is an experienced professional in the field of clinical trial management and eTMF systems. Currently serving as an eTMF Manager at KLIFO A/S since October 2021, Jessica is responsible for updating eTMF SOPs and implementing Veeva Vault eTMF functionalities. Previously, Jessica held roles at LEO Pharma as both a Clinical Support Specialist - Associate Professional and Senior Coordinator, where contributions included eTMF optimization, document management, and training of CRO staff. Jessica’s career also includes a QA Assistant position at Caldic Ingredients Denmark A/S and research roles at the University of Copenhagen, where Jessica participated in trials focused on physical activity and nutrition. Jessica holds degrees in Human Biology and Food Science and Nutrition from the University of Copenhagen.
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KLIFO
KLIFO is an integrated North-European drug development consultancy with significant experience in partnering with pharmaceutical and biotech companies. We enable our partners to maximise opportunity, mitigate risks, drive innovation and achieve efficient project advancement. We offer end to end solutions across all drug development areas, including strategic project management, regulatory affairs, clinical development, clinical trial supply, quality assurance (QA), Chemistry Manufacturing and Controls (CMC) development, non-clinical development and pharmacovigilance in relation to the development of pharmaceutical products. We provide strategic advice as well as operational support in all these areas, and we partner with clients on portfolio strategies, project development strategies and project execution. KLIFO has offices in Denmark, Sweden, Germany and The Netherlands and employs more than 150 highly skilled employees.