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I come from an academic background in the field of biosciences and have experience in managing clinical research studies and science communication. I have strong interpersonal, communication and organisational skills. I enjoy taking on challenges and setting myself the highest career goals I believe I can achieve.

Experiences

Past Experience

  • Egg Donation & Communications Officer London, UK

    January 2018 --- June 2019

  • Clinical Study Manager London, UK

    October 2015 --- October 2017

Personality

Self Assessment :
Attention to detailAdaptabilityAnalytical thinkingApproachabilityAuthenticityCharmCollaborationCommunicativeCoordinationCritical thinkingCuriosityDependabilityDiligenceFlexibilityIndependenceInterest in knowledgeOrganizationPerspectiveProactivityProblem solvingResponsibilitySelf-disciplineSelf-disclosureStrategic thinkingTrustWillingness to compromise

Knowledge

Self Assessment :
Animal models Biochemistry Biostatistics Cell biology Diabetes R&D Scientific writingActions and modes of action of human physiologyAdverse Events (AE)Animal trialBiologyBiomedical SciencesBiotechnologyCell biologyCellular Product DevelopmentCell SignalingClinical Data ManagementClinical researchClinical Study DesignClinical trial designClinical trial managementClinical Trial SuppliesCommunication SkillsData AnalysisDeveloping Clinical Trial ProtocolsDNA extractionEnglishGastroenterologyGeneticsGenomicsGood Clinical Practice (GCP)GraphPad PrismLaboratory ResearchLaboratory study designLife SciencesLiquid chromatographyMedical writingMetabolismMicrosoft ExcelMitigationMolecular geneticsMonitoring Study ProgressPhysiologyPre-clinical researchProject CoordinationProject PlanningProject ManagementScientific CommunicationsScientific WritingSearch literature on clinical trialsSoftware DocumentationSocial SkillsSPSSStandard Operating Procedure (SOP)Statistical Data Analysis

Skills and Expertise

Self Assessment :
Analyze data Analytical skills Build and manage the Trial Master File (TMF) Create SOPs Develop clinical trial protocols Develop protocols Guide students Interact with nurses Interact with physicians Interpret data Molecular Diagnostics Monitor a clinical study Search literature on clinical trials Write papers Write protocolsAnalyze data/information to determine potential relationships.Approve patient informationArchive documentationArchive trial documentation and correspondence.Archive study documentsAseptic techniquesAssess adverse reactionsAssist study siteAssist with experimentsAssist with proceduresAssist with site trainingAttend seminars, courses and meetings within and outside the companyBuild trial master file (TMF)Calculate trial timelinesClinical data collectionCoach and provide guidance to clinical staff.Collaborate with project teamCollaborate with principal investigatorCommunicate effectively on different company levelsCollect patient forms and questionnairesCommunicationConduct animal studiesConduct literature searchesConduct limited data and/or statistical analysis.Conduct research at universitiesConduct site initiationCreate clinical project documents according to the protocolCreate standard operating procedure (SOP)Distribute trial suppliesDistribute study documentsdrafting grant applicationsEnsure good clinical practice (GCP)Establish contractsEstablish professional relationships with partnersEstablish relationships with Key Opinion LeadersIdentify investigatorsIdentify sitesInteract with pre-clinical scientistsInteract with statisticiansInterpret analytical resultsInterpret scientific dataLiaise with doctors and other professionals throughout the studyManuscript preparationManuscript preparation and reviewOral presentationOversee data collectionParticipate in medical review

Education

  • PhD in Biosciences from King’s College London in 2017
  • Master in Reproductive and Developmental Biology from Imperial College London in 2013
  • Bachelor in Cell and Molecular Biology from Universidade Nova de Lisboa in 2011

Languages

BrightOwl Assessment:
Self Assessment:
Portuguese
Native
English
Full Proficiency
Spanish
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA) Medical Science Liaison (MSL) Associate Scientist Scientific Associate Biologist Clinical Laboratory Technician Clinical Research Coordinator Clinical Research Manager Clinical Trial Assistant (CTA) Clinical Trial Coordinator (CTC) Clinical Trial Manager (CTM) Clinical Trial Specialist (CTS) CRM Doctoral Researcher Field Project Manager Freelance Science Writer Lab Scientist Medical translator Medical Writer Molecular Biologist Post-doctoral Fellow Postdoctoral fellow Postdoctoral Research Fellow Preclinical Project Manager Preclinical Research Manager Preclinical Scientist Project Assistant R&D Scientist Research associate Research fellow researcher Sample Coordinator Scientific Advisor scientific collaborator Scientific consultant Scientific Officer Scientific Researcher scientific translator Scientific Writer Scientist Translator
  • Locations I am interested in:
    Lisbon, Portugal
  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl freelancer :    40 Hours per week
    BrightOwl employee
  • International:
    Yes

Publications

    Expert has 2 publications (Will be avalible with full profile)

Area / Region

Lisbon, Portugal

Others

Driving License
  • No

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