Senior Clinical Research Associate

Yesterday

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Business Wire

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

501 - 1000

Description

• Executing clinical monitoring activities at clinical trial sites • Monitoring clinical trials in accordance with ICH guidelines and GCP • May be assigned to CRA activities or start-up activities, depending on experience • Performing feasibility, site identification, selection and evaluation

Requirements

• Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines • 2-5 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 German and English (writing and speaking)

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