Clinical Research Associate I

November 4

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Business Wire

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

501 - 1000

Description

• Complete the requirements of the BeiGene CRA Training Program (12-14 weeks) • Conduct site visits and function as the site manager. • Monitor data quality and patient safety through monitoring and site education. • Complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs. • Provide audit/inspection preparation support to clinical study sites.

Requirements

• Fluent in English and Portuguese. • Spanish is a plus. • Experience in Pharmaceutical/Biotech Industry, Hematology, Oncology preferred. • Excellent communication and interpersonal skills. • Excellent organizational skills and ability to prioritize and multi-task. • BS/BA in a relevant scientific discipline. • 5+ years of relevant Clinical Operations experience or 1+ years in a clinical research associate position is preferred.

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