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CRA I – CRA II – FSP in Deutschland
Location
DeutschlandSalary
NegotiableContract
PermanentWe are currently recruiting for CRA I - CRA IIs in the south of Germany on behalf of a key client of ours, an industry leader in the clinical research market, where the candidate will be outsourced in a client dedicated position for a top-biopharma sponsor working in projects in both Oncology and Vaccines.
As a Clinical Research Associate, you will:
- Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service on multiple, challenging projects.
- Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work.
- Perform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently.
- Benefit from award winning training programmes that will assist your technical and professional skills and knowledge.
Education and Experience:
- University degree in a life-sciences field
- Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation
- Demonstrated understanding of ICH-GCP, EU and FDA requirements
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Exceptional communication, collaboration, organisational and time management skills
- Excellent command of German and English language
Disclaimer:
This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission.
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