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Past Experience

  • Clinical Research Associate (CRA) Barcelona, Spain

    May 2014 --- January 2015

    monitoring Clinical research studies on oncology phse iv.

  • Clinical Research Associate (CRA)

    April 2013 --- May 2014

    monitoring Clinical research studies on reumathology and oncology Phase III.

  • Career advisor Barcelona, Spain

    January 2012 --- June 2012

    development of actions of individual counseling and group aimed at the unemployed. provide information and guidance counselor work. management job offer and candidates.

  • Clinical Research Associate (CRA) Barcelona, Spain

    September 2008 --- October 2010

    monitoring Clinical research studies on oncology Phase III.

  • Clinical Research Associate (CRA) Barcelona, Spain

    September 2007 --- December 2007
    monitoring international Clinical research studies on Central nervous system (CNS)Phase III.

  • Clinical Research Associate (CRA) Barcelona, Spain

    November 2006 --- September 2007


    monitoring Clinical research studies on Dermatology.

  • Clinical Trial Assistant (CTA) Barcelona, Spain

    July 2005 --- November 2006

    Clinical Trial assistant in Clinical trials Phase III in Central nervous system (CNS).

  • Psychologist Barcelona, Spain

    July 2004 --- January 2005

    interviews with healthy aging population, patients with mild cognitive impairment and dementia. screening and neuropsychological assessment. cognitive rehabilitation. psychological and emotional support.

  • Clinical Data Manager (DM) Barcelona, Spain

    September 1999 --- August 2003

    management of patients with dementia and mild cognitive impairment (mci). cognitive screening and neuropsychological assessment of Clinical Trial patients. Research in Neuroscience, medical Publications and data results.


  • Psychologist Virginia, USA

    May 1999 --- August 1999

    psychological and emotional support to patients with mental illness and brain injury.

  • Career advisor Barcelona, Spain

    November 1998 --- March 1999

    development of actions of individual counseling and group (iobes), designed to promote the employability of unemployed. provide information and guidance counselor work. management of job offer.

  • Career advisor Barcelona, Spain

    May 1998 --- September 1998

    Training in skills of labor insertion aimed at the unemployed and working population. interviews and management of job offer.

  • Career advisor Barcelona, Spain

    October 1995 --- September 1997

    user management, individual and group interviews and psychological evaluation with psychometric tests, writing and returning psychological assessment reports, orientation and guidance.   


  • Elementary School English Teacher Barcelona, Spain

    January 1997 --- June 1997

    English classes to children with eight, eleven and thirteen years of age. preparation of material and exam revision

  • Psychologist in Human Resources Barcelona, Spain

    May 1996 --- May 1997
    group interviews and psychological evaluation with psychometric tests. writing and returning reports of personnel selection.


  • Psychologist Tarragona, Spain

    December 1993 --- August 1994

    psychological and emotional support for children and teenager with social and family breakdown.


Self Assessment :
Analytical thinkingAttention to detailCommunicativeIndependenceInterest in knowledgeAdaptabilityProblem solvingKindnessCreative thinkingCritical thinkingCollaboration


LinkedIn Assessment :
Clinical trialsClinical researchGCPICH-GCPCROoncologyLifesciencesRegulatory submissionsClinical monitoringMedical writingRegulatory affairsCTMSSOPProtocolControl clPharmaceutical Industry

Skills and Expertise

Self Assessment :
Create SOPs Develop protocols Report data Search literature on clinical trials Write papers Write protocolsAct as the main line of communication between the sponsor and the investigatorAdministrative supportAdverse event reportingAlzheimerAnalyze data/information to determine potential relationships.Archive documentationArchive study documentsArchive trial documentation and correspondence.Assess site feasibilityAssist study siteAssist with proceduresAssist with routine testsAssure medical qualityAttend investigator meetingClinical data collectionCoach and provide guidance to clinical staff.Coach clinical staffcollaborate in research projects at universitiesCollaborate with medical teamCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Collaborate with principal investigatorCollaborate with project teamCollect dataCollect financial data from hospitalsCollect patient forms and questionnairesCommunicate effectively on different company levelsCommunicate with investigatorCommunicate with sponsorCommunicationCompile informationComplete case report form (CRF)Complete study proceduresConduct close-out visitsConduct literature searchesConduct literature searches.Conduct maintenance visitsConduct site initiationConfirm protocol complianceContact potential subjectsContract approvalControl protocol versionsData entryData verificationDistribute study documentsDistribute trial suppliesEnsure data consistencyEnsure data integrityEnsure good clinical practice (GCP)Establish relationships with Key Opinion LeadersEstimate subject complianceEthics committee applicationEthics committee submissionsGastrointestinal diseasesIdentify investigatorsIdentify sitesInformed consent processInitiate clinical trials Interact with CROsInteract with ethics committeeInteract with nursesInteract with physiciansInteract with pharmacistsInteract with pre-clinical scientistsInteract with regulatory stakeholdersInteract with statisticiansInterpret scientific dataLiaise with doctorslifescienceMonitor dataMonitoring enrolmentMonitoring subject complianceNegotiationOral presentationPeople managementPresent clinical resultsProvide trainingPublication of articlesRead medical literatureRegulatory documentationRegulatory submissionsResolves queriesRespond to audit findingsReview clinical study reportsReview exclusion criteriaReview inclusion criteriaReview informed consent processReview manufacturing documentationReview medical reportsReview monitoring reportsReview protocolsSerious Adverse Event (SAE) ReconciliationSite managementSolve problemsTeachingTrain off site staffTrain on site staffUnderstand protocolsVerify dataWrite final reportsWrite papersWritten presentation


  • Authorized by the Department of Health of the Government of Catalonia in General Health Psychologist from Universidad de Barcelona in 2015
  • Postgraduate course in Psychooncology from Institut Superior d’Estudis Psicològics (ISEP). in 2008
  • Postgraduate course in Research and Development: Clinical Research Associate from Foundation ESAME. in 2005
  • Postgraduate in Cognitive Rehabilitation from Instituto Superior de Estudios Psicológicos (ISEP) in 2004
  • Postgraduate in Psicogeriatry from Instituto Superior de Estudios Psicológicos (ISEP) in 2003
  • Certificate of Research Proficiency in The doctor degree of Neuro-sciences. from Barcelona Medicine Faculty. University of Barcelona. in 2002
  • Postgraduated in Labour insertion from Institut Superior d’Estudis Psicològics (ISEP). in 1997
  • Bachelor Degree in Psychology from School of Psychology. University of Barcelona. in 1995


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Medical translator Medical Writer Scientific Writer Study Start-up Specialist Translator scientific collaborator Regulatory Affairs Associate Junior Recruitment Consultant
  • Locations I am interested in:
    Barcelona, Spain
  • Work From Home:
    Yes, 5 Days
  • Work Regime:
    Permanent position :    0.5% FTE
    BrightOwl freelancer :    25 hours Hours per week
    BrightOwl employee :    0.5% FTE
  • International:


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

Area / Region

Barcelona, Spain


Driving License
  • Yes

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