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Administracja biurowa » Pracownik biurowy

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CRA/Senior CRA Opportunity, Growing European CRO, Cologne or Home base Nr ref.: /JOBS.pl Ideal for CRA I/II with 1+ years Clinical Research experience, and a fluency in German and English, A growing independent European CRO with operations across Central and Eastern Europe. We have forged a fantastic reputation for our quality approach and the fantastic service provided by our highly skilled and experienced Clinical department which is largely made up of Physicians and PhDs. We have established an extensive client base, comprised of some of the top 10 global Pharmaceutical organisations alongside niche Biotechnology and leading Medical Device organisations. This extensive client base means we cover a hugely varied range of complex studies including Oncology, Cardiovascular, Ophthalmology and Paediatric studies from phase I-IV. We pride ourselves on developing highly skilled study teams with therapeutic and country specific experience dedicated to suiting our client's needs. As a smaller growing CRO we are able to show a lot of flexibility in adapting to specific requirements of our clients meaning we can take on many complex studies that larger CROs are simply unable to! It also means we can offer a flat hierarchy with a clear route of communication to senior management and much quicker development to management! Full job description and company details are available upon application, apply below. This position is being dealt with Russell Smith at meet, for further details, please call on or email directly at to discuss in confidence. Company Background • Growing European CRO • Internationally recognised for our highly innovative and adaptable approach • Award winning clinical study team • Rapidly expanding with offices across Europe. • Focus on providing Phase I-IV clinical trials services to the pharmaceutical, biotech and medical device industries. • Specialist in the Cardiovascular, Oncology and Paediatric Studies • Excellent training and support provides incredible opportunities for career progression and personal development • Highly competitive salary (€45,000 - €65,000 P/A plus benefits) For further details, please call on or email directly at to discuss in confidence. 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 1 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 For further details, please 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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