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 Team in Argentina and are currently seeking to hire a CRA II. This is a permanent, full time position.
The opportunity to work within an experienced and highly skilled team.
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 :
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.
g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
Thorough knowledge of monitoring procedures
Basic understanding of the clinical trial process
Valid Driver's License
Thorough knowledge of Company SOPs regarding site monitoring
Experience : Minimum Required :
Minimum Required :
A minimum of 1 (One) year of Clinical Monitoring experience is preferred, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job can be substituted.
Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, and local regulatory 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
Ability to work with minimal supervision
Good communication and interpersonal skills
Good analytical and negotiation skills
Fluent in local office language and in English, both written and verbal
Works efficiently and effectively in a matrix environment
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, however an equivalent combination of education and experience to successfully perform the key responsibilities of the job.