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
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
Fluent in local office language and in English, both written and verbal
Work efficiently and effectively in a matrix environment