Clinical Research Associate

November 29

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Business Wire

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

501 - 1000 employees

Founded 1961

Description

• Execute clinical monitoring activities at clinical trial sites. • Ensure clinical trials are conducted according to ICH guidelines and GCP. • Collaborate with clinical operations to ensure study timelines are met and quality standards are maintained.

Requirements

• Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines. • Ideally 2+ 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. • Fluent in English (writing and speaking).

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