Clinical Research Associate I Bogota Cundinamarca
Covance
Bogota, Cundinamarca, co
hace 17 horas
source : Ecadoo

Job Overview COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries We are recruiting for our Flexible Sourcing team in Colombia and are currently seeking to hire a CRA I This is a permanent full time position Covance s ongoing success offers team members unsurpassed growth and career development opportunities At Covance we help make the miracles of medicine a reality We offer opportunities to work on diverse challenging projects with bright interesting colleagues while building a flexible and rewarding career This is your chance to become part of a team that helps to bring miracle of medicine to market sooner There is no better time to join us Education Qualifications Minimum Required External Candidates University or college degree or certification in a related allied health profession from an appropriately accredited institution e g nursing licensure AND A minimum of six months on site monitoring preferred Internal candidates Internal candidates with a minimum of 6 months of experience as a Clinical Research Assistant or Internal candidates with a minimum 2 years clinical trials or site management experience e g study coordinator project coordinator project specialist study start up Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements Basic understanding of the clinical trial process Valid Driver s License Preferred Working knowledge of Covance SOPs for site monitoring Experience Experience Minimum Required External Candidates o University or college degree or certification in a related allied health profession from an appropriately accredited institution e g nursing licensure AND o a minimum of six months of on site monitoring preferred Internal candidates o Internal candidates with a minimum of 6 months of experience as a Clinical Research Assistant OR o Internal candidates with a minimum 2 years clinical trials or site management experience e g study coordinator project coordinator project specialist study start up Ability to monitor study sites according to protocol monitoring guidelines SOPs ICH Guidelines and GCP Ability to work within a project team Good planning organization and problem solving abilities Good communication skills oral and written Good computer skills Works efficiently and effectively in a matrix environment Fluent in local office language and in English both written and verbal Preferred One 1 or more additional years of experience in a related field i e medical clinical pharmaceutical laboratory research data analysis data management or technical writing is preferred

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