Senior Clinical Research Associate

October 2

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Business Wire

Public Relations • Press Release Distribution • Investor Relations • SEC filing • SEO

501 - 1000

Description

• The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. • Collaborates with the Clinical Study Teams (CSTs) by supporting day-to-day clinical study activities. • Proactively seeks opportunities to lead and drive improvements.

Requirements

• 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

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