BrightOwl Loader Loading

Emil Hoeck is an ambitious, high-performing professional with excellent analytical, strategic and interpersonal skill sets. Emil started his career in 2012 at a Clinical Research Site as a patient-facing clinical trial assistant after which he transitioned into Quality Assurance in a highly specialized Clinical Research Organization, a department in which he ended up having the overall responsibility for. Building upon his previous experience, Emil is currently building Strategic Site Relationships globally in a Top 3 CRO, collaborating with and managing internal and external stakeholders. With a Master of Science in Medicine with Industrial Specialization focusing on Translational Medicine, Emil has a strong, broad medical background and extensive experience in managing all aspects of clinical trials in an academic setting. Emil has published research papers in British Journal of Dermatology and Experimental Dermatology, as well as a three-part monthly series on patient centricity in clinical trials in industry newsletter CenterWactch.


Current Experience

  • Manager

    Since November 2018
    Account Manager

    Key account manager for strategic Sites and Institutions within Early Phase Oncology, Ophthalmology, Pediatrics as part of the Catalyst Program, Syneos Health's strategic site relationship program.
    Responsible for delivering data analyses to support selection of new strategic sites for the Catalyst Networks
    Responsible for the data-driven evaluation of Catalyst Network performance on clinical trials
    Responsible for development and maintenance of the Team's reporting tools, enabling Key Performance Indicators to be reported to Senior Management.
    Business Unit liaison to Business Technology for the ongoing development of Syneos Health's Investigator Portal "Connect for Investigative Sites"


Past Experience

  • Senior Specialist Denmark

    July 2017 --- November 2018
    business unit

  • Site & Patient Coordinator Camberley, UK

    July 2016 --- June 2017

    Helped establish the on-site evaluation tool for the Catalyst Program, the Company's preferred site relationship program
    Conducted on-site evaluation of sites considered for the Catalyst Vaccine Network
    Authored a 3-part series on patient centricity published in CenterWatch


  • Director of Quality Assurance Denmark

    October 2015 --- June 2016
    Quality Management System

  • QA Associate Denmark

    January 2013 --- September 2015
    Quality System

  • Clinical Research Assistant Denmark

    September 2012 --- January 2013
    Clinical Trial


Self Assessment :
Attention to detailApproachabilityCharmCollaborationCommunicativeDiligenceCuriosityEfficiencyIndependenceInnovative thinkingInterest in knowledgeOptimismOrganizationProactivityProblem solvingPerspectiveResiliencyResult OrientedResponsibilitySelf-confidenceSelf-disciplineSociabilityStrategic thinkingTrustAdaptabilityFlexibility


Self Assessment :
Clinical DevelopmentClinical monitoringClinical pharmacologyClinical operationsClinical researchClinical Study DesignClinical trial budgetingClinical trial managementClinical trialsGood Clinical Practice (GCP)Account ManagementKOL managementRisk ManagementTime ManagementChange ManagementProject ManagementInformation Management SystemsKey Account ManagementClinical Trial Management System (CTMS)International Project ManagementData AnalysisData cleaningStatistical Data AnalysisAnalysisVaccinesPsychiatryPediatricsoncologyOphthalmology
LinkedIn Assessment :
Quality AssuranceClinical researchClinical trialsPhase IPhase IIGCPMicrosoft OSPSSPharmaceutical IndustryLife SciencesmanagementMedical DevicesSOPValidationGMPGLPClinical Development

Skills and Expertise

Self Assessment :
Analytical skills Analyze data Create SOPs Interact with physicians Interact with nurses Interpret data Search literature on clinical trials Report data Write papersAdjust methodsAdjust processes Adjust processes and methodsAssess site feasibilityAssist study siteAssist with site trainingCollaborate with medical teamCollaborate with project teamCollaborate with principal investigatorCommunicate effectively on different company levelsCommunicate with investigatorCommunicationComplete study proceduresConduct university research Data miningDesign clinical trialDesign data collection systemsDesign data reporting systemsDesign marketing advertismentsDetermine statistical analysis Determine potential relationshipsDevelop ICH/GCP compliant processesDevelop strong internal relationships with stakeholdersDevelop training materialsDirect co-workers to achieve resultIdentify investigatorsImplement data collection systemImplement data reporting systemsImplement Key Performance Indicators (KPI's)Indentify clinicians to conduct clinical trialsInteract with computer specialistsInteract with CROsInteract with KOLInteract with nursesInteract with physiciansInterpret dataLiaise with doctorsLiaise with professionals in other divisions of the company as requiredMaintain strong relationshipsMaintain Quality Management System (QMS)Maintenance of biomedical equipmentManage multiple projectsMonitor Key Performance Indicators (KPI's)Negotiate budget NetworkObserve trends in dataOral presentationOrganise meetingsPresent data at congressproject managementProvide trainingPublication of articlesReport Key Performance Indicators (KPI's)Review dataSite managementSupport due diligence assessmentsTrain on site staffTrain StaffTranslate strategy into operational plansWork cross-functionallyWork collaboratively with the other members of the clinical research team Written presentation


  • Master of Science, in Medicine with Industrial Specialization - Translational Medicine Profile from Aalborg Universitet in 2017
  • Bachelor of Science in Medicine with Industrial Specialization from Aalborg Universitet in 2015

Training and Certification

  • Lean Six Sigma Yellow Belt in 2017 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Elementary Proficiency
Elementary Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Manager Clinical Research Associate (CRA) Lead Consultant Medical Science Liaison (MSL) Medical Writer Product Manager Product Specialist Project Leader Project Manager Account Manager Account Manager - Life Sciences Clinical Trial Manager (CTM)
  • Positions I am NOT interested in:
    Qa QA Consultant QA Engineer QA Lead QA Officer QC/QA Manager Quality Assurance (QA) Manager Quality Engineer Quality manager
  • Locations I am interested in:
    Denmark Madrid, Spain Munich, Germany Spain Switzerland Zürich, Switzerland
  • Work From Home:
    Yes, 1 to 3 days per week
  • Work Regime:
    Permanent position
  • International:


    Expert has 5 publications (Will be avalible with full profile)

Area / Region



Driving License
  • Yes

Similar Candidates

Other Candidates in Denmark

Other similar Candidates in this location (country / city)

Other Candidates

Most Recent Searches

Most Famous Searches

You might also like