Senior Clinical Research Associate

September 20

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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

Description

• Manage, deliver and/or perform full clinical site monitoring services for one or more projects. • Responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management. • Act as primary liaison between CRAs and project team and participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents, and tools. • Assist with selection, hiring, training, and supervision of CRAs as needed. • Identify and recruit site investigators, coordinate the movement and delivery of trial materials. • Facilitate and support site staff with access to study systems and ensure sites are compliant with project specific training requirements. • Oversee overall integrity of the study and promote positive working relationships with the site and staff.

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

Benefits

• Home-based • Regular travel