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Experience Study coordinator trained to manage clinical trials led by the Pharmaceutical Industry.

That is the domain where I look forward to working closely with, striving to achieve their most ambitious goals.

As to my character I would highlight an excellent organisational capacity, good comunication skills and goal oriented personality.




Current Experience

  • Study Coordinator
    Since May 2015

    I have worked as a Study coordinator in the Digestive Unit of the Virgen Macarena Hospital.

    My commitment was to manage all the clinical trials carried out there; being the intermedary between the pharmaceutical industry and the medical department so that everything was done in accordance with the established Protocol.

    Clinical Trial´s Documentation and Protocol management, assistance to nurse and physicians with procedures, data collection and interaction with patients have been some of my most frecuent daily activities.

    Diseases in which most of the research is conducted are Crohn´s Disease and Ulcerative Colitis. Autoinmune diseases whose origin and cure today is unknown are the challenge for the Pharmaceutical Industry.

Past Experience

  • Farmacéutica Facultativa
    August 2014 --- August 2014
    Trabajé como farmacéutica facultativa tomando nueva experiencia en la realización de las tareas propias del farmacéutico.

  • Farmacéutica Adjunta
    March 2014 --- May 2014
    Trabajé como farmacéutica adjunta reemplazando a la titular en las tareas propias de la misma como la firma de documentos así como el resto de tareas propias de farmacéutico.

  • Farmacéutica
    February 2013 --- July 2013
    Trabajé como farmacéutica facultativa ganando mucha experiencia en una farmacia que por sus dimensiones y su horario 24 horas me enseñó a trabajar de una forma eficiente sin perder calidad en el trato con los clientes.


Self Assessment :
ApproachabilityAdaptabilityAuthenticityCharmCommunicativeCritical thinkingDiligenceInterest in knowledgeKindnessOrganizationProblem solvingSociabilityService orientedStriving


LinkedIn Assessment :
Mi formaciComo puntos fuertes puedo destacar mi constancia y seriedad en el trabajo, la faIndustria FarmacInglEnsayos clEstrategia empresarialEspaBiotecnologInvestigaciLiderazgo de equiposCiencias naturalesInvestigaci

Skills and Expertise

Self Assessment :
Control data Interact with nurses Interact with physicians Interpret data Report dataAdverse event reportingArchive documentationArchive study documentsCollaborate with medical teamCollaborate with principal investigatorAttend investigator meetingContact potential subjectsData entryEnsure good clinical practice (GCP)Patient recruitmentProtocol managementReview queriesReview inclusion criteriaReview exclusion criteriaAssist with proceduresClinical data collectionCollect patient forms and questionnairesCommunicate with investigatorGastrointestinal diseases


  • Monitor de Ensayos Clínicos in from Fundación ESAME in 2015
  • Licenciada en Farmacia in from Facultad de Farmacia de la Universidad de Sevilla in 2013

Training and Certification

  • Monitoriación de ensayos clínicos in 2015 Certification
  • Licenciada en Farmacia in 2013 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Data Manager (DM) Clinical Research Coordinator Clinical Research Associate (CRA) Clinical Trial Assistant (CTA) Data Manager Drug Safety Officer Data Reviewer Global Data Manager Clinical Research Associate (CRA) Pharmacist Pharmacovigilance Assistant Pharmacovigilance Officer
  • Locations I am interested in:
    England, United Kingdom France Spain United States
  • Work From Home:
  • Work Regime:
    Permanent position :    70%-90% FTE
    BrightOwl freelancer :    50%-70% Hours per week
    BrightOwl employee :    70%-90% FTE
  • International:

Area / Region



Driving License
  • Yes