Recruiter Information

7689 www.clinicalprofessionals.eu
Daniel patterson
Marketing Associate
0044 (0)118 9594990

DocJob

  • J115333
  • Clinical Research Associate - Hungary Top salary + company package
  • Permanent
  • Clinical Research Associate - Hungary Top salary + company package
    Permanent position
    Office based Budapest


    Company Overview

    Our client is a leading international CRO with a focus on delivering efficiency and consistent value in all that they do. Through their global reach and therapeutic expertise this company have fostered the development of highly successful partnerships with a number of top ranking Pharmaceutical companies.

    Job Summary
    Monitoring for Phase I-IV clinical research studies while developing an understanding of the drug development process, GCP, and relevant regulations. Management of study site activities and ensure adherence to regulatory guidelines and SOPs

    Key Duties
    • Performs feasibility, pre-study site visits, study start-up, clinical trial initiation, monitoring and close out activities in accordance with regulations and SOPs.
    • Develops new approaches for site selection, and pre-study activities and completes site evaluation
    • Completes submission of documents to the Ethics Committees and tracks regulatory documents. Manages investigator grants.
    • Develops monitoring plan, CRFs, and other study related documents.
    • Preparation and coordination of investigator meetings and attends when required.
    • Develops patient enrollment strategies.
    • Ensures proper storage, dispensation, and accountability of all Investigational Products
    • Completes study site closeout visits and study site evaluation

    Skills and Education:
    RN, BSc or equivalent
    At least 2 years clinical trial monitoring experience
    Good command of written and spoken English and Hungarian (essential).
    Ability to travel domestically and internationally as required
    Exp in Cardiovascular studies

    If this opportunity is of interest please contact Ed Bezer +44 207 822 1710 ed.bezer@clinicalprofessionals.eu

    Clinical Professionals is an equal opportunities employer. Please only apply to this opportunities if you are legally able to live and work in Bulgaria and have the required linguistic ability as these are essential to the role.

    Keywords Hungary Budapest CRA SCRA Monitoring Permanent Officebased Clinical Research Klinikai kutatási Magyarország Clinical Research Associate Cardiovascular CNS Oncology
  • August 04, 2012

  • Company Overview

    Our client is a leading international CRO with a focus on delivering efficiency and consistent value in all that they do. Through their global reach and therapeutic expertise this company have fostered the development of highly successful partnerships with a number of top ranking Pharmaceutical companies.

    Job Summary
    Monitoring for Phase I-IV clinical research studies while developing an understanding of the drug development process, GCP, and relevant regulations. Management of study site activities and ensure adherence to regulatory guidelines and SOPs

    Key Duties
    • Performs feasibility, pre-study site visits, study start-up, clinical trial initiation, monitoring and close out activities in accordance with regulations and SOPs.
    • Develops new approaches for site selection, and pre-study activities and completes site evaluation
    • Completes submission of documents to the Ethics Committees and tracks regulatory documents. Manages investigator grants.
    • Develops monitoring plan, CRFs, and other study related documents.
    • Preparation and coordination of investigator meetings and attends when required.
    • Develops patient enrollment strategies.
    • Ensures proper storage, dispensation, and accountability of all Investigational Products
    • Completes study site closeout visits and study site evaluation

    Skills and Education:
    RN, BSc or equivalent
    At least 2 years clinical trial monitoring experience
    Good command of written and spoken English and Hungarian (essential).
    Ability to travel domestically and internationally as required
    Exp in Cardiovascular studies

    If this opportunity is of interest please contact Ed Bezer +44 207 822 1710 ed.bezer@clinicalprofessionals.eu

    Clinical Professionals is an equal opportunities employer. Please only apply to this opportunities if you are legally able to live and work in Bulgaria and have the required linguistic ability as these are essential to the role.

    Keywords Hungary Budapest CRA SCRA Monitoring Permanent Officebased Clinical Research Klinikai kutatási Magyarország Clinical Research Associate Cardiovascular CNS Oncology
An EU passport or work permit is required for this position. Applicants without one of these will be rejected automatically.
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