Clinical Research Associate, (CRA - SCRA) Global Medical Device Organi Nr ref.: /JOBS.pl Ideal for CRAs with 2+ years' experience an interest in Medical Device Studies and a fluency in German and English, As a Global leader in the development of Medical Device solutions for Cardiovascular Diseases, we have a global presence throughout Europe, Asia, Africa and the Americas. We have now been established for over 50 years in which time have gained an outstanding reputation for our innovative approach and high levels quality. You will be joining a highly skilled and ambitious Clinical team, with the opportunity to work across a range of highly complex and scientific Clinical Studies dealing with devices at the forefront of the industry. As the successful candidate you can expect a huge investment in your training and development with a clear route through to management positions. We hold an impressive record of internal promotion for our management and have incredibly high staff satisfaction scores alongside one of the lowest staff turnover rates in the industry. Full job description and company details are available upon application, apply below. This position is being dealt with Russell Smith at meet, call on or email directly at to discuss in confidence. Company Background • Global Leading Medical Device organisation • Internationally recognised for a highly innovative approach • A Specialist in the development of devices within the Cardiovascular field • Excellent training and support provides incredible opportunities for career progression and personal development • Highly competitive salary (€50,000 - €60,000 P/A plus Company Car) If you have any questions at all call Russell Smith on or email directly at . As the successful candidate you can expect the following responsibilities: · Full Monitoring responsibilities to ensure trials operate in adherence to all ICH-GCP and internal SOPs · Site management · Assisting with study protocol design · All types of monitoring visit · Opportunity to work directly with one of the top 10 Global Pharma's and Biotech's Skills Required · Min 2 years' independent monitoring experience · Fluent in German, good knowledge of English · Profound knowledge of all ICH-GCP Protocol and any local regulations · Ability to work from home within Germany Full job description and company details are available upon application, apply below. This position is being dealt with Russell Smith at meet, call on or email directly at to discuss in confidence. Find out more about us at Meet are good people who are great at recruitment. We're proud to partner with the industry's leading Pharmaceutical, Biotechnology, Medical Device, Marketing Communications and Contract Research Organisations (CROs) worldwide, helping them to find and secure the best global talent available. We pride ourselves on our open, friendly approach and are here to guide you through the recruitment process every step of the way. Find out more about us at Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .
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