Athena Lemesiou

Senior Client Success Manager, EMEA at Ada Health
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Contact Information
us****@****om
(386) 825-5501
Location
Cyprus, CY
Languages
  • Greek Native or bilingual proficiency
  • English Native or bilingual proficiency
  • French Limited working proficiency
  • Italian Elementary proficiency
  • Spanish Elementary proficiency

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Experience

    • Germany
    • Hospitals and Health Care
    • 200 - 300 Employee
    • Senior Client Success Manager, EMEA
      • Jan 2022 - Present

    • Client Success Manager, EMEA
      • Sep 2018 - Jan 2022

    • Business Development Manager, Global
      • Aug 2017 - Sep 2018

      Ada is a global health company founded by doctors, scientists, and industry pioneers to create new possibilities for personal health. Ada’s core system connects medical knowledge with intelligent technology to help all people actively manage their health and medical professionals to deliver effective care. Ada is proud to collaborate with leading health systems and global non-profit organizations to carry out this vision.

    • United Kingdom
    • Technology, Information and Internet
    • 1 - 100 Employee
    • Advisor
      • Apr 2017 - Aug 2018

      Vertical Future is a vertical farming company based in London that builds, designs and engineers automated controlled-environment agriculture (CEA) systems. http://verticalfuture.co.uk/ Vertical Future is a vertical farming company based in London that builds, designs and engineers automated controlled-environment agriculture (CEA) systems. http://verticalfuture.co.uk/

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Associate Project Manager - Patient recruitment and retention
      • Jun 2016 - Aug 2017

      • Supporting the pharmaceutical industry with patient recruitment and retention in clinical trials • Co-coordinating and optimizing marketing strategies • Tracking project deliverables ensuring timelines and recruitment targets are met and are within budget • Engaging with internal departments and external vendors and ensuring coordination of work • Organizing and running internal and external meetings, taking and circulating minutes, developing agendas and… Show more • Supporting the pharmaceutical industry with patient recruitment and retention in clinical trials • Co-coordinating and optimizing marketing strategies • Tracking project deliverables ensuring timelines and recruitment targets are met and are within budget • Engaging with internal departments and external vendors and ensuring coordination of work • Organizing and running internal and external meetings, taking and circulating minutes, developing agendas and presentations • Developing and maintaining relationships with clients Show less • Supporting the pharmaceutical industry with patient recruitment and retention in clinical trials • Co-coordinating and optimizing marketing strategies • Tracking project deliverables ensuring timelines and recruitment targets are met and are within budget • Engaging with internal departments and external vendors and ensuring coordination of work • Organizing and running internal and external meetings, taking and circulating minutes, developing agendas and… Show more • Supporting the pharmaceutical industry with patient recruitment and retention in clinical trials • Co-coordinating and optimizing marketing strategies • Tracking project deliverables ensuring timelines and recruitment targets are met and are within budget • Engaging with internal departments and external vendors and ensuring coordination of work • Organizing and running internal and external meetings, taking and circulating minutes, developing agendas and presentations • Developing and maintaining relationships with clients Show less

    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Medical Writer
      • Sep 2015 - Jun 2016

    • Associate Medical Writer
      • Mar 2014 - Sep 2015

    • United Kingdom
    • Research Services
    • 700 & Above Employee
    • PhD researcher in Clinical Epilepsy
      • Oct 2010 - Sep 2014

      • Investigated three different methods (invasive and non-invasive) of identifying epileptogenic areas in pharmacoresistant epilepsy patients assessed for surgical candidacy • Responsible for setting up the study at Queen Square and King’s College Hospital by establishing ethics and R&D approvals and by training hospital staff • Designed the study protocol, patient information sheet and consent form • Screened and recruited patients, collected and analysed data (icEEG, SPES, MEG) and… Show more • Investigated three different methods (invasive and non-invasive) of identifying epileptogenic areas in pharmacoresistant epilepsy patients assessed for surgical candidacy • Responsible for setting up the study at Queen Square and King’s College Hospital by establishing ethics and R&D approvals and by training hospital staff • Designed the study protocol, patient information sheet and consent form • Screened and recruited patients, collected and analysed data (icEEG, SPES, MEG) and wrote the thesis • Presented work at international conferences and gave internal presentations • Facilitated focus groups of PhD students • Tutored Year 1 medical students Three year full scholarship (2010-2013) from Epilepsy Research UK (ERUK) Conference presentations: European Congress of Epileptology (ECE) London 2012, American Epilepsy Society (AES) San Diego 2012 Software: Nicolet, Fasst, Curry7, BrainVision Analyzer, Neuroarchiver, Microsoft Word, SPSS, Excel, STATA Show less • Investigated three different methods (invasive and non-invasive) of identifying epileptogenic areas in pharmacoresistant epilepsy patients assessed for surgical candidacy • Responsible for setting up the study at Queen Square and King’s College Hospital by establishing ethics and R&D approvals and by training hospital staff • Designed the study protocol, patient information sheet and consent form • Screened and recruited patients, collected and analysed data (icEEG, SPES, MEG) and… Show more • Investigated three different methods (invasive and non-invasive) of identifying epileptogenic areas in pharmacoresistant epilepsy patients assessed for surgical candidacy • Responsible for setting up the study at Queen Square and King’s College Hospital by establishing ethics and R&D approvals and by training hospital staff • Designed the study protocol, patient information sheet and consent form • Screened and recruited patients, collected and analysed data (icEEG, SPES, MEG) and wrote the thesis • Presented work at international conferences and gave internal presentations • Facilitated focus groups of PhD students • Tutored Year 1 medical students Three year full scholarship (2010-2013) from Epilepsy Research UK (ERUK) Conference presentations: European Congress of Epileptology (ECE) London 2012, American Epilepsy Society (AES) San Diego 2012 Software: Nicolet, Fasst, Curry7, BrainVision Analyzer, Neuroarchiver, Microsoft Word, SPSS, Excel, STATA Show less

    • Hospitals and Health Care
    • 1 - 100 Employee
    • Medical Interpreter
      • May 2013 - Mar 2014

      Professional Face-to-Face Interpreter between Greek/Cypriot patients and NHS clinicians Professional Face-to-Face Interpreter between Greek/Cypriot patients and NHS clinicians

    • United Kingdom
    • Translation and Localization
    • 200 - 300 Employee
    • Medical Interpreter
      • Mar 2013 - Mar 2014

      Professional Face-to-Face Interpreter between Greek/Cypriot patients and NHS clinicians Professional Face-to-Face Interpreter between Greek/Cypriot patients and NHS clinicians

  • Thames Stroke Research Network
    • London, United Kingdom
    • Stroke Research Practitioner
      • Nov 2009 - Jul 2010

      •Charing Cross and St Mary's Hospitals •Established necessary procedures for the opening of new clinical trials (R & D, Ethics applications) •Educated/trained staff on the portfolio of clinical trials by writing SOPs, creating PowerPoint presentations and ward posters •Screened stroke patients and evaluated eligibility for recruitment into suitable trials •Communicated with patients/families to provide verbal/written information and obtained informed… Show more •Charing Cross and St Mary's Hospitals •Established necessary procedures for the opening of new clinical trials (R & D, Ethics applications) •Educated/trained staff on the portfolio of clinical trials by writing SOPs, creating PowerPoint presentations and ward posters •Screened stroke patients and evaluated eligibility for recruitment into suitable trials •Communicated with patients/families to provide verbal/written information and obtained informed consent •Registered/randomised patients onto study protocols •Collected relevant data, completed case report forms and transferred them to trial centres •Documented trial data, created and maintained site files in conformance with ICH GCP guidelines and within appropriate timelines •Organised MDT meetings and agendas •Contributed to the creation of Patient and Public Involvement (PPI) brochures Training and certificates: ICH GCP, Information Governance NIH Stroke Scale, Stroke Core Competencies, Modified Rankin scale Phlebotomy (UCLH certificate) Show less •Charing Cross and St Mary's Hospitals •Established necessary procedures for the opening of new clinical trials (R & D, Ethics applications) •Educated/trained staff on the portfolio of clinical trials by writing SOPs, creating PowerPoint presentations and ward posters •Screened stroke patients and evaluated eligibility for recruitment into suitable trials •Communicated with patients/families to provide verbal/written information and obtained informed… Show more •Charing Cross and St Mary's Hospitals •Established necessary procedures for the opening of new clinical trials (R & D, Ethics applications) •Educated/trained staff on the portfolio of clinical trials by writing SOPs, creating PowerPoint presentations and ward posters •Screened stroke patients and evaluated eligibility for recruitment into suitable trials •Communicated with patients/families to provide verbal/written information and obtained informed consent •Registered/randomised patients onto study protocols •Collected relevant data, completed case report forms and transferred them to trial centres •Documented trial data, created and maintained site files in conformance with ICH GCP guidelines and within appropriate timelines •Organised MDT meetings and agendas •Contributed to the creation of Patient and Public Involvement (PPI) brochures Training and certificates: ICH GCP, Information Governance NIH Stroke Scale, Stroke Core Competencies, Modified Rankin scale Phlebotomy (UCLH certificate) Show less

    • Cyprus
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Research Internship
      • Jun 2007 - Sep 2007

      Department of Clinical Neurophysiology Research project: A new neurogenic vestibular evoked potential (N6) recorded with the use of air-conducted sound Department of Clinical Neurophysiology Research project: A new neurogenic vestibular evoked potential (N6) recorded with the use of air-conducted sound

    • Cyprus
    • Hospitals and Health Care
    • 100 - 200 Employee
    • Clinical Physiology trainee
      • Jun 2006 - Sep 2006

      Department of Clinical Neurophysiology Observation of Electromyography, Electroencephalography (routine/video), Nerve conduction studies, Evoked potentials, Polysomnography, Vagus nerve stimulation, Neuropathology Laboratories Department of Clinical Neurophysiology Observation of Electromyography, Electroencephalography (routine/video), Nerve conduction studies, Evoked potentials, Polysomnography, Vagus nerve stimulation, Neuropathology Laboratories

Education

  • University College London, U. of London
    Doctor of Philosophy (PhD), Clinical Epilepsy
    2010 - 2014
  • University College London, U. of London
    Master of Science (MSc), Clinical Neuroscience
    2008 - 2009
  • The University of Manchester
    Bachelor of Science (BSc), Neuroscience
    2004 - 2008

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