Clinical Research Associate

We are seeking Clinical Research Associates (CRAs) to conduct site monitoring responsibilities for Clinical trials. The CRAs will be responsible for all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, and other duties.

Requirements

• Minimum of two (2) years of clinical research monitoring experience
• Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
• Good planning, organization and problem solving abilities
• Ability to work with minimal supervision
• Good communication and interpersonal skills
• Good analytical and negotiation skills
• Computer competency
• Fluent in local office language and in English, both written and verbal

Benefits

• EEO Employer: Company is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran)
• Confidentiality and privacy are important to us