Senior Clinical Research Associate

November 14

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Business Wire

Public Relations β€’ Press Release Distribution β€’ Investor Relations β€’ SEC filing β€’ SEO

501 - 1000 employees

Founded 1961

Description

β€’ Primarily a site monitor responsible for management and oversight of clinical study sites β€’ Ensures data quality and patient safety in accordance with ICH-GCP guidelines β€’ Collaborates with Clinical Study Teams and provides mentoring to CRA team members β€’ Develops collaborative relationships with investigative sites and study vendors β€’ Tracks enrollment and study-specific status reports to ensure compliance and timely delivery of milestones

Requirements

β€’ BS/BA in a relevant scientific discipline β€’ Minimum of 4-6 years of relevant Clinical Operations experience β€’ Minimum of 3-4 years of (CRA) monitoring experience in the pharmaceutical or CRO Industry β€’ Excellent communication and interpersonal skills β€’ Excellent organizational skills and ability to prioritize and multi-task

Benefits

β€’ Medical β€’ Dental β€’ Vision β€’ 401(k) β€’ FSA/HSA β€’ Life Insurance β€’ Paid Time Off β€’ Wellness

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