Sr Clin Res Assoc

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 Argentina and are currently seeking to hire a SR. CRA. 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:University or college degree, or certification in related allied health profession from an appropriately accredited institution (e.g. nursing licensure) Thorough knowledge of CGP-ICH and basic understanding of the regulatory requirements Fluent in English and Spanish

 Experience:A minimum of 4 years of Clinical Monitoring experience Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines 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 Good communication and interpersonal skills Computer competency Fluent in local office language and in English, both written and verbal Work efficiently and effectively in a matrix environment