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- Pharmacist with experience in Pharmaceutical Industry in the areas of Clinical operations, Quality Control and production. - these experiences have developed my ability to adapt to change, and quickly assuming new responsibilities. - pro-active and self-motivated professional, focused on meeting goals. high attention to detail and performing well under pressure ensuring all tasks are completed. - systemic Coaching master’s degree ability to observe how relationships affect the quality of work, so capable of team buildings skills and excellent communications skills.


Past Experience

  • Registered Pharmacist

    January 2014 --- August 2014
    • worked to legal and ethical guidelines to ensure the correct and safe supply of medical products to the general public. • provision of advice and information for maintaining and improving people’s Health, including the supply of prescription medicines as appropriate. • checked blood pressure monitoring, cholesterol monitoring and Diabetes screening.

  • Control Supervisor Specialty Gases Laboratory

    September 2007 --- March 2013
    • managed the daily gas production process, reducing product delivery time up 2 weeks and responding the urgent needs of customers. • managed the quality assessment in the Laboratory, to meet GMP in the areas of medical gases and Medical Devices, iso17025 and safety and environment standards. • managed Human Resources and scheduling of staff, achieving the highest performance in filling gases, and Analysis. • responsible for the Planning of the Laboratory activities, including the Verification and calibration of equipment. • responsible for the purchase of raw materials and for the quality of the finished product. • investigation and resolution on both internal and customer complaints.

  • CRA in oncology clinical trials

    March 2005 --- September 2007
    • monitored Phase II Clinical trials in oncology. • performed site initiation, monitoring and close-out visits. • prepared submissions for the Ethics committee and managed the notifications. • developed and prepared study documents: crfs, study document templates and legal documents and contracts with Hospitals. • coordinated all aspects of the Clinical monitoring process in accordance with gcps, sops and the monitoring plan. • handled and notified saes, aes, science)" rel="nofollow">Protocol violations. • drug Procurement)" rel="nofollow">Supply Management: monitored drug accountability log and dispensation log. • supplied study materials to the sites, including samples and device shipment. • data query resolution tracking. • management of payments relating to tests and treatments.

  • Registered Pharmacist

    January 2001 --- January 2005


Self Assessment :
Creative thinkingAttention to detailOrganizationOrientationProblem solvingResiliencyEmotional reactivityCritical thinking


LinkedIn Assessment :
CoachingHolistic HealthMindfulness MeditationConfigurationsoncologyClinical researchClinical DevelopmentClinical Data ManagementClinical monitoringClinical trialsPharmaceutical IndustryPharmacovigilanceRegulatory affairsGMPQuality Assurance (QA)Quality Control (QC)CROGCPEnsayos clFarmacovigilanciaIndustria FarmacInvestigaciDesarrollo clAsuntos normativosBuena prSOPGestiProtocol


  • Master In Systemic Coaching in Office Management from Autonomous University of Barcelona in 2013
  • Master in International Development Clinical Trials in Pharmaceutical sciences from IUSC & Barcelona University in 2005
  • Pharmacist in Pharmaceutical sciences from Barcelona University in 2002


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Area / Region

London, United Kingdom


Driving License
  • No

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