Senior Clinical Research Associate

3 days ago

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501 - 1000

Description

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

Requirements

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

Benefits

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