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Administracja biurowa » Pracownik biurowy

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Opis:

Covance Spain is looking for Clinical Research Associates - up to EUR Nr ref.: /JOBS.pl Our Clinical divisions currently have several needs for Clinical Research Associates. Locations : Madrid (office-based) / Barcelona (home-based) - Outsourcing division ° CRAs (2 to 4 yrs experience including oncology) - home-based - Madrid and Barcelona : - Internal Clinical Operations division ° CRAs (min 1 yr monitoring experience) - office-based - Madrid - Early Clinical Development division (ECD) ° CRA (min 2 yrs monitoring experience, phase I - II a plus) - home-based Profile : University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) A minimum of 1 up to 4 years clinical monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) - oncology experience would be a plus for all vacancies Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines A full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Fluency in English and local language Good communication, planning, organization and problem solving skills Your rewards: Up to a EUR 10,000 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 Education/Qualifications: University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements Thorough knowledge of monitoring procedures Basic understanding of the clinical trial process Experience: Minimum 1 up to 5 years of monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) - oncology experience highly preferred. Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Oncology experience is a definite plus Experience with phase I would be appreciated for the ECD division Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Good planning, organization and problem solving abilities Ability to work with minimal supervision Good communication and interpersonal skills Good analytical and negotiation skills Computer competency Fluent in English and local language, both written and verbal Works efficiently and effectively in a matrix environment Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us. Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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