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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, protocol violations. • Drug 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