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vision always willing to adjust to our client’s requirements by the Innovation of our services. mission to ensure and guarantee the patients security and integrity, via data veracity and the right fulfillment of the good clinical practices. goal that all our monser monitors will act in each project in an optimal manner, carrying out an effective autonomous task, while being capable of becoming part of and offering results within a multidisciplinary team; achieving with each project an increase in their knowledge, profile, and ability to solve problems through an appropriate theoretical formation, practical experience, and management duties.

 about monsermonser s.a.  costa rica headquaters

is a private group of independent Clinical Research Associates (cras), with broad experience in clinical studies. we are a multidisciplinary team, whose members have participated in many research projects of phases ii, iii and iv from major Pharmaceutical companies, providing services related to the development and progress of Health and Medicine, with Operations since 2004 in central, south america, the caribbean and mexico. at the same time, we are able to provide different types of services besides study monitoring, according to your particular needs.


Current Experience

  • Senior Clinical Research Associate

    Since February 2004

Past Experience

  • Senior Clinical Research Associate

    February 2002 --- March 2012


Self Assessment :
AdaptabilityAggressivenessApproachabilityAttention to detailCollaborationCoordinationCreative thinking


LinkedIn Assessment :
PlanificaciBuena prNormas ICH de buenas prControl clEnsayos clOrganizaciLiderazgo de equiposMicrosoft ExcelSistema de gestiDesarrollo cl

Skills and Expertise

Self Assessment :
Act as the main line of communication between the sponsor and the investigator Build and manage the Trial Master File (TMF) Create SOPs Develop clinical trial protocols Analyze data Build the CMC development plan Assure medical quality Guide students Interact with physicians Monitor a clinical studyApprove drug supply Archive documentationApprove consent documentsAssist study siteAssign activitiesAssess site feasibilityAttend investigator meetingAttend seminarsCalculate trial timelinesCoach staffCollaborate with principal investigatorCollect patient forms and questionnairesConduct monitor visitsCoordinate logisticsCreate clinical documentsCreate economic parametersDesign trial master file (TMF)Develop ICH/GCP compliant processesFollow-up of external auditsInteract with CROsManage clinical trial files/documentsPre-study procedures Ensure good clinical practice (GCP)


  • in from Universidad Latina de Costa Rica in 0000

Training and Certification

  • SENIOR CRA in 2007 Training
  • SENIOR CRA in 2007 Certification

Work Preferences

  • Work From Home:
  • Work Regime:
    Permanent position :    40% FTE
    BrightOwl freelancer :    30 Hours per week
    BrightOwl employee :    40% FTE
  • International:

Area / Region

San José, Costa Rica


Driving License
  • Yes

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