Clinical Research

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations, and standards
• Coordinate activities required to set up and monitor studies
• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits
• Travel to sites for monitoring visits
• Identify potential study risks and propose mitigation solutions
• Prepare for investigator meetings, site visits, and project team updates
• Handle conflicts using resolution strategies
• Take responsibility for work quality and outcomes

Explore Clinical Research Associate I – Clinical Research Associate II at Precision For Medicine. Review requirements and application details.

Clinical Research Associate I – Clinical Research Associate II

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