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Clinical Research Associate - Spain - Oferta z Jobs.pl

Administracja biurowa » Pracownik biurowy

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Clinical Research Associate - Spain

Nr ref.: /JOBS.pl

  • I am currently working exclusively with a a Global CRO outsourced to a market leading pharmaceutical company looking for a Clinical research associate for a regional monitoring opportunity in Spain.

    This role will be office based in Madrid

    I am interested in talking to experienced Clinical Research Associate/Senior Clinical Research Associates.

    The CRA is accountable for conducting monitoring activities of assigned clinical trials. You will work proactively in identifying, resolving/mitigating and escalating risks and/or issues.

    Key responsibilities:

    Monitoring with a focus on data integrity and patient safety
    Plans day to day activities for monitoring of a clinical study and sets priorities per site
    On-site qualification, study initiation, interim monitoring and close-out monitoring visits at investigator sites
    Reducing backlog and keeping it at a minimum
    Escalates issues and feedback for the team
    Provides accurate and timely submission of trip reports
    Assists project team with assessing project feasibility and recruitment
    Participates in Investigators' Meeting
    Ensures adherence to study timeline and budget
    Mentoring and training junior level staff as required
    Participating in available training offered to increase therapeutic knowledge

    Ideal Profile:

    Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
    Previous on-site monitoring experience is essential
    Fluent English
    Knowledge of ICH / GCP regulations
    Excellent team player, collaborative and able to enable an effective team
    Excellent organizational and time-management skills, able to meet deadlines
    Self-starter with lots of common sense and able to act on own initiative
    Maintains a positive, results orientated work environment
    Travel: 70-85%
    Valid driver's license, passport as required

    This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be. Please contact Sayful Islam on (O) or email a CV to .com.

    Keywords: Clinical Research Associate Senior CRA project manager contract clinical trials CRA II clinical research clinical cra, scra, cpm, clinical, clinical research, clinical research associate, pharmaceuticals, biotech, cro, pharma, senior clinical research associate. UK, United Kingdom, England, Scotland, Wales, Northern Ireland


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