As a Senior Study Manager, I coordinate the processes of preparing and tracking clinical trials, data processing activities and market research; effectively streamlining GCP/ISO, quality, regulatory, privacy and legal processes. I aim for full compliance with processes and regulations, while keeping a flexible and pragmatic attitude; thus enabling the researcher to answer the relevant research questions optimally while still being fully compliant.
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Clinical Trial Project ManagerEcraidEindhoven, Nb, Nl -
Senior Study ManagerPhilips Jan 2021 - PresentSupervising the comprehensive management of clinical, privacy, legal, security, and regulatory aspects across Philips Personal Health Research projects at a program level: Released and unreleased non-medical devices as well as released medical devices, conducted at Philips' internal and external study sites. -
Research ScientistPhilips Sep 2010 - Jan 2021High Tech CampusLeading and executing projects connected to sleep and chronobiology, with the focus on (clinical) trials, product development and testing. 2013-2020: member of the CTO Works Council; secretary of the Daily Governance, member of the Health and Safety committee (chair 2013-2015). and communication committee. -
Brain Bank AssistantThe Netherlands Brain Bank Mar 2007 - Aug 2010Amsterdam, North Holland, NetherlandsAssisting the Brain Bank researcher and the pathologist in collecting human brain tissue of donors with a variety of neurological and psychiatric disorders. -
Phd StudentNetherlands Institute For Neuroscience Feb 2005 - Aug 2010Amsterdam Area, NetherlandsTitle: Circadian rhythm deterioration in early Alzheimer disease and the preventive effects of light.Preparing and executing a double blind, placebo controlled clinical trial (longitudinal study); responsible for data collection logistics and processing, statistical analysis and reporting. The research study examined circadian rhythm changes in Alzheimer's Disease, as well as the effect of longitudinal exposure of light therapy in patients with Alzheimer's Disease and congitive… Show more Title: Circadian rhythm deterioration in early Alzheimer disease and the preventive effects of light.Preparing and executing a double blind, placebo controlled clinical trial (longitudinal study); responsible for data collection logistics and processing, statistical analysis and reporting. The research study examined circadian rhythm changes in Alzheimer's Disease, as well as the effect of longitudinal exposure of light therapy in patients with Alzheimer's Disease and congitive disorders. The study was executed at the Alzheimer Centre of the VU Medical Hospital. Show less -
Research AssistantRijksuniversiteit Groningen Jan 2004 - Dec 2004Groningen, NetherlandsResponsible for the daily logistics of human research studies, in the field of sleep and circadian research. Performing accompanying (radiactive) laboratory work (RIA's) and statistical analyzes.
Els Møst Education Details
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The Graduate School Neurosciences Amsterdam Rotterdam (Onwar)Neuroscience -
Phd School Of Chronobiology -
Neurobiology And Behavior -
Experimental Psychiatry -
Chronobiology
Frequently Asked Questions about Els Møst
What company does Els Møst work for?
Els Møst works for Ecraid
What is Els Møst's role at the current company?
Els Møst's current role is Clinical Trial Project Manager.
What schools did Els Møst attend?
Els Møst attended The Graduate School Neurosciences Amsterdam Rotterdam (Onwar), Phd School Of Chronobiology, University Of Groningen, University Of Pennsylvania, University Of Groningen.
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