Lead CRA, International Mid-sized European CRO, Office based, Frankfur Nr ref.: /JOBS.pl Suitable for CRAs and SCRAs with 4 years of monitoring experience, looking to take the next step up towards a Lead CRA role. This is an opportunity for an experienced CRA/SCRA to join an innovative and successful organisation with a Global reach spanning across over 20 European countries, North and South America, Middle East, Asia and Australia. We are experienced in phase I-IV clinical studies across a variety of indications, specialising in Oncology, Neurology and Orphan Diseases. We searching for a proactive and driven CRA with 4 years' monitoring experience, we can offer the right candidate the opportunity to take on lead CRA responsibilities. There is a set structure of progression for all CRAs with a clear route through to Clinical trial management, within a feasible time frame. You will directly report to the director of Clinical Operations and join a growing team able to offer outstanding support and training as you transition from a CRA through to management. 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 · Leading international European CRO with a presence across over 40 countries · Phase I through to late phase studies · Huge variety of indications including Oncology, Orphan Drugs and Neurology · Excellent training and support provides incredible opportunities for career progression and personal development · Excellent company atmosphere with clear communication lines · Highly competitive basic salary Please call Russell Smith at meet, call on or email directly at for further details. Role Responsibilities · Full Monitoring responsibilities to ensure trials operate in adherence to all ICH-GCP and internal SOPs · Additional Lead responsibility, responsible for guiding and leading CRAs · Clinical Trial Management responsibilities · Site management · Assisting with study protocol design · All types of monitoring visit Call Russell Smith at meet, call on or email directly at for further details. Skills required 4 years Monitoring experience · Fluent in German, good knowledge of English · Profound knowledge of all ICH-GCP Protocol and any local regulations · Ability to work from the office in Frankfurt 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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