Clinical Research Associate

Please enter in the e-mail title following details:
CRA/country/last name_first name

Summary of Job Specification:
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines

Travel Required:

• Available for travel from 50% to 80% of the time, including overnight stays as necessary, consistent with project needs and office location
• Ability to drive and have a valid driver’s license

Education / Qualifications Required:

• 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)
• Knowledge of GCP, monitoring procedures, basic understanding of regulatory requirements

Experience / Skills Required:

• Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
• Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, GCP
• Good planning, organization and problem solving abilities