Clinical Research Associate II or III - Ulm

My client, a very successful mid-size American CRO with different locations in Europe and the European headquarters located inUlmis looking for an experienced CRA candidate (2+ years) to assist on multi-centre clinical trials inGermany. The position is officebased and can later be turned to homebased. The company offers excellent training as well as personal and career development opportunities in this expanding company. Furthermore, careful selection of employees has ensured an open, friendly and fun working environment and the company enjoys a very low staff turnover rate. Tasks: Planning, co-ordination and overviewing of all monitoring activities of clinical trials to ensure the highest quality, that time-frames are met, communication with the client etc. The trials will be conducted inGermanyas part of international projects to GCP Company standards. It is also of extreme importance to handle submissions to the regulatory authorities. Requirements: * Minimum of 2 years experience as a CRA working on Phase II to IV trials in at least one of the following indications: oncology, virology, immunology, transplantation medicine, gene-therapy, cell-therapy * Fluency in German, excellent English * In depth knowledge of FDA and ICH GCP requirements * Excellent communication skills and computer literacy * Willingness to travel inGermanyon a regular basis * Willing to work officebased inUlm My client offers the opportunity to work at the highest level in a respected international organisation. This is a permanent full time position with attractive basic salary, bonus and add-ons. Please note that a company car is not provided. If you meet the specifications above and wish to apply for the position, please attach your CV in English via the link given and do not forget to mention your notice period as well as your availability for a phone call from my side. Das biete ich Ihnen: * Drei Jahre Erfahrung im deutschen Pharmamarkt - exzellente Marktkenntnisse, sehr dichtes Netzwerk an Kontakten aus der Klinischen Forschung * Kompetente, seriöse Beratung vom ersten Kontakt bis lang nach der Vermittlung * Ihre Daten sind geschützt: Ihr CV wird nicht ohne gemeinsame Absprache und Ihre Erlaubnis weitergeleitet * Interviewvorbereitung * Unterstützung mit und bei Vertragsverhandlungen Kontakt: ALEKSANDRA STOJANOVIC, (M.A,) , Principal Consultant Clinical Operations b>+49 89 551 9766