Clinical Research Associate ||

The Clinical Research Associate will serve as the primary point of contact for investigative sites, providing contextual information on clinical trials and connecting stakeholders to sites. They will align and motivate site staff, conduct site evaluations, and ensure compliance with regulations and quality standards.

Requirements

• Primary Sponsor point of contact for investigative sites
• Aligns, trains, and motivates site staff with support as needed
• Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure activities
• Customizes site engagement strategy for assigned study(ies)
• Evaluates and ensures effective recruitment and retention techniques/plans
• Responsible for continuous risk-assessment and monitors activities conducted by clinical sites
• Identifies, evaluates, and recommends new/potential investigators/sites
• Ensures quality of data submitted from study sites and assures timely submission of data
• Ensures audit and regulatory inspection readiness at assigned clinical site
• Manages investigator payments as per executed contract obligations

Benefits

• Equal Opportunity Employer
• Committed to operating with integrity, driving innovation, transforming lives, and serving the community