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Administracja biurowa » Pracownik biurowy

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CIVANCE ITALY has several CRA opportunities for you in various regions Nr ref.: /JOBS.pl Do you know Covance is the world´s leading Central Laboratory services provider and one of the most stable, fastest growing global Contract Research Organization? For example, our Clinical Development teams have supported the development of one-third of all prescription medicines in the market today and of 47 out of the 50 best-selling oncology drugs. The work we do at Covance impact the lives of millions of people around the world… so could you too as our next! Covance has several CRA opportunities for you in various regions of Italy: this is a great moment to join us! - up to EUR 5000 Sign on Bonus! Locations: Rome / Milan(home-based) and well communicated centers in Italy Our Early Clinical Development division (ECD) is looking for Clinical Research Associates in oncology: - 2 - 3 years of Experience in a related field, including 1 - 2 years Clinical Monitoring Experience with Phase I and PoC Studies We need CRA II who are ready to apply their pre-study, initiation, monitoring and closeout visits expertise, and their deep ICH-GCP and SAE management expertise to bring safe, effective and essential medicines to market sooner. Your rewards: ° Up to a EUR 5,000 sign on bonus - limited time only, apply now! ° The opportunity to pursue further training and an interesting career in an inspiring environment that values achievement, supports a balance between your personal and professional life and allows you to make meaningful contributions ° Flexible conditions and an attractive remuneration package Interested candidates have to transmit their personal cv according to the Italian legislative decree n° 196/2003 Education/Qualifications - University/college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology). - Thorough knowledge of ICH guidelines, GCP and the clinical trial process - Knowledge of the drug development process. - Proficient computer skills with good working knowledge of a range of computer packages including Electronic CRF processes. - Excellent verbal and written communication skills - Valid Drivers License Experience - 2 - 3 years of Experience in a related field, including 1 - 2 years Clinical Monitoring Experience - Experience with Phase I and PoC Studies EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us. Regional, ITA Regional, Italy Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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