Senior Clinical Research Associate
Yesterday
Description
• Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale. • In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices. • In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and tools. • Represents the corporation by maintaining collaborative relationships with stakeholders.
Requirements
• The successful candidate will possess a minimum of a college diploma/degree and 4-6 years of related experience. • The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results. • Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results. • Ability to engage in continuous learning and self-development. • Ability to continually foster teamwork. • Fluent in the reading, writing and speaking of English
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